ClinVar Miner

List of variants reported as likely benign for acne inversa, familial, 1

Included ClinVar conditions (1):

Acne inversa, familial, 1

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
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_015331.3(NCSTN):c.1101+13T>C	rs41266885	0.00907
NM_015331.3(NCSTN):c.1249A>T (p.Asn417Tyr)	rs143039637	0.00277
NM_015331.3(NCSTN):c.437-12C>G	rs201416838	0.00019

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