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Links from Gene

Items: 70

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ARID3B
(P329S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARID3B
(A410G)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARID3B
(Q17H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARID3B
(Q17E)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARID3B
(M466T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADPGK, ARID3B
+29 more
Deletion
Brugada syndrome 8
GUncertain significance
ARID3B, C15orf39
+47 more
Deletion
Pyogenic arthritis-pyoderma gangrenosum-acne syndrome
GUncertain significance
ARID3B
(A164T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARID3B
(K159E)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARID3B
(S551G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARID3B
(S532G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARID3B
(R417G)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARID3B, CLK3
+14 more
Copy number gain
not specified
GUncertain significance
ADPGK, ARID3B
+48 more
Copy number loss
Chromosome 15q24 deletion syndrome
GPathogenic
ARID3B
(G472S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARID3B
(K208E)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
AAGAB, ABHD17C
+209 more
Copy number gain
not provided
GPathogenic
ARID3B
(S54F)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARID3B
(R462Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADPGK, ARID3B
+29 more
Duplication
Bardet-Biedl syndrome
GUncertain significance
ARID3B
(W190R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARID3B
(V227I)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
ARID3B
(Q130E)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARID3B
(G350R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARID3B
(R328W)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARID3B
(R447C)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARID3B
(Q5E)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARID3B
(P147S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARID3B
(I491S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARID3B
(P166L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARID3B
(R402C)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARID3B
(G350A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARID3B, C15orf39
+48 more
Copy number loss
not provided
GPathogenic
ARID3B, C15orf39
+34 more
Copy number loss
Hearing impairment
GPathogenic
ADPGK, ARID3B
+41 more
Deletion
not provided
GPathogenic
CGNL1, MAPDA
+472 more
Duplication
Familial colorectal cancer
+1 more
GUncertain significance
ARID3B, C15orf39
+34 more
Copy number loss
not provided
GPathogenic
ADPGK, ARID3B
+37 more
Copy number loss
not provided
GPathogenic
ARID3B
Single nucleotide variant
(synonymous variant)
not provided
GBenign
ARID3B
Single nucleotide variant
(synonymous variant)
not provided
GBenign
ARID3B
Single nucleotide variant
(synonymous variant)
not provided
GBenign
ADPGK, ARID3B
+36 more
Copy number loss
not provided
GPathogenic
ADPGK, ARID3B
+47 more
Copy number gain
not provided
GPathogenic
ADPGK, ARID3B
+36 more
Copy number loss
not provided
GPathogenic
ADPGK, ARID3B
+48 more
Copy number loss
not provided
GPathogenic
ABHD17C, ABHD2
+215 more
Copy number gain
not provided
GPathogenic
ADPGK, ARID3B
+37 more
Deletion
not provided
GPathogenic
PDIA3, PEAK1
+521 more
Duplication
not provided
GPathogenic
MIR6882, MPI
+258 more
Duplication
Schizophrenia
GLikely pathogenic
LOC130057525, LOC130057526
+205 more
Duplication
Schizophrenia
GLikely pathogenic
ADPGK, ARID3B
+37 more
Copy number loss
See cases
GPathogenic
AAGAB, ABHD17C
+559 more
Copy number gain
See cases
GPathogenic
NOX5, NPAP1
+559 more
Copy number gain
See cases
GPathogenic
ADPGK, STOML1
+48 more
Copy number loss
not provided
Gnot provided
CHRFAM7A, CHRM5
+566 more
Copy number gain
See cases
GPathogenic
ALDH1A2, ALDH1A3
+444 more
Copy number gain
See cases
GPathogenic
WHAMM, CCNB2
+308 more
Copy number gain
not provided
GLikely pathogenic
ARID3B, C15orf39
+49 more
Copy number gain
See cases
GUncertain significance
ADPGK, ARID3B
+47 more
Copy number gain
See cases
GPathogenic
ADPGK, ARID3B
+37 more
Copy number loss
See cases
GPathogenic
AAGAB, ABHD17C
+278 more
Copy number gain
See cases
GPathogenic
LOC116268473, LOC116268474
+1244 more
Copy number gain
See cases
GPathogenic
LOC130057927, LOC130057928
+1764 more
Copy number gain
See cases
GPathogenic
LOC130057584, LOC130057585
+202 more
Copy number loss
See cases
GPathogenic
ACSBG1, ADPGK
+487 more
Copy number loss
See cases
GPathogenic
LOC130057567, LOC130057568
+243 more
Copy number loss
See cases
GPathogenic
ARID3B, LOC121530592
+5 more
Copy number gain
See cases
GLikely benign
ADPGK, ADPGK-AS1
+195 more
Copy number loss
See cases
GLikely pathogenic
ADPGK, ADPGK-AS1
+204 more
Copy number gain
See cases
GPathogenic
ADPGK, ADPGK-AS1
+236 more
Copy number loss
See cases
GPathogenic
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