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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
WASHC5, WASHC5-AS1
Single nucleotide variant
(intron variant)
Ritscher-Schinzel syndrome
+4 more
GBenign/Likely benign
WASHC5, WASHC5-AS1
(R859C +1 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
WASHC5-related condition
+3 more
GUncertain significance