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Links from OMIM

Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CDKN2A
Microsatellite
(inframe_insertion +2 more)
not provided
+5 more
GPathogenic/Likely pathogenic
CDKN2A
(M53I +2 more)
Single nucleotide variant
(missense variant +1 more)
Melanoma and neural system tumor syndrome
+3 more
GPathogenic
CDKN2A
(G101W +2 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+6 more
GPathogenic
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