List of variants in gene KRT13 reported as uncertain significance for White sponge nevus 2

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_153490.3(KRT13):c.*228C>G	rs574184263	0.00022
NM_153490.3(KRT13):c.759G>C (p.Gln253His)	rs766894151	0.00004
NM_153490.3(KRT13):c.*175G>A	rs1459808765	0.00003
NM_153490.3(KRT13):c.1350C>T (p.Arg450=)	rs140142101	0.00003
NM_153490.3(KRT13):c.991C>T (p.Leu331=)	rs771435962	0.00003
NM_153490.3(KRT13):c.1295C>G (p.Ser432Cys)	rs1394162514	0.00002
NM_153490.3(KRT13):c.*74A>C	rs886052907	0.00001
NM_153490.3(KRT13):c.1220G>A (p.Ser407Asn)	rs1265435884	0.00001
NM_153490.3(KRT13):c.337G>A (p.Asp113Asn)	rs886052908	0.00001
NM_153490.3(KRT13):c.496-9A>G	rs780820686	0.00001
NM_153490.3(KRT13):c.823G>A (p.Ala275Thr)	rs767618537	0.00001
NM_153490.3(KRT13):c.*162T>C	rs1904829902
NM_153490.3(KRT13):c.*19C>T	rs760565338
NM_153490.3(KRT13):c.*85C>T	rs886052906
NM_153490.3(KRT13):c.523C>G (p.Arg175Gly)	rs764088068
NM_153490.3(KRT13):c.853G>A (p.Ala285Thr)	rs1904920258

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