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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
WASHC5, WASHC5-AS1
Single nucleotide variant
(synonymous variant)
not provided
+3 more
GLikely benign
WASHC5, WASHC5-AS1
(S784T +1 more)
Single nucleotide variant
(missense variant)
Ritscher-Schinzel syndrome
+2 more
GUncertain significance
WASHC5, WASHC5-AS1
(F882V +1 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not provided
GUncertain significance
WASHC5-AS1, WASHC5
Single nucleotide variant
(non-coding transcript variant +1 more)
not provided
+3 more
GConflicting classifications of pathogenicity
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