List of variants in gene ADAR reported as likely pathogenic for Symmetrical dyschromatosis of extremities

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001111.5(ADAR):c.2885+1G>A
NM_001111.5(ADAR):c.3019G>A (p.Gly1007Arg)	rs398122822
NM_001111.5(ADAR):c.3143T>C (p.Leu1048Pro)	rs1571050825

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