List of variants in gene KCTD1 reported as likely benign for Scalp-ear-nipple syndrome

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_001142730.3(KCTD1):c.2181C>T (p.Pro727=)	rs180735402	0.00016
NM_001142730.3(KCTD1):c.220G>T (p.Asp74Tyr)
NM_001142730.3(KCTD1):c.2440-3C>T

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