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Links from MedGen

Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CACNA1A
Deletion
(3 prime UTR variant +1 more)
Specific learning disability
+12 more
GConflicting classifications of pathogenicity
TNFRSF13B
(R20C)
Single nucleotide variant
(missense variant)
Abnormal basal ganglia MRI signal intensity
+12 more
GUncertain significance
DNAH7
(F3585L)
Single nucleotide variant
(missense variant)
Abnormal muscle tone
+4 more
GPathogenic
IFIH1
(R779H)
Single nucleotide variant
(missense variant)
Aicardi-Goutieres syndrome 7
+10 more
GPathogenic/Likely pathogenic
BMPR2
(G182D)
Single nucleotide variant
(missense variant)
Pulmonary arterial hypertension
GLikely benign
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