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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HERC2
(V4538M)
Single nucleotide variant
(missense variant)
Prader-Willi syndrome
+3 more
GUncertain significance
HERC2
(R2800H)
Single nucleotide variant
(missense variant)
Developmental delay with autism spectrum disorder and gait instability
+3 more
GUncertain significance
HERC2
(M1792V)
Single nucleotide variant
(missense variant)
not provided
+4 more
GUncertain significance
HERC2
Single nucleotide variant
(synonymous variant)
not provided
+3 more
GLikely benign
HERC2
(R1045C)
Single nucleotide variant
(missense variant)
Prader-Willi syndrome
+3 more
GLikely benign
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