rs60440396

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(T;T)	0	common in clinvar

Make rs60440396(C;C)

Make rs60440396(C;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

41505195

Gene

KRT13

is a	snp
is	mentioned by
dbSNP	rs60440396
dbSNP (classic)	rs60440396
ClinGen	rs60440396
ebi	rs60440396
HLI	rs60440396
Exac	rs60440396
Gnomad	rs60440396
Varsome	rs60440396
LitVar	rs60440396
Map	rs60440396
PheGenI	rs60440396
Biobank	rs60440396
1000 genomes	rs60440396
hgdp	rs60440396
ensembl	rs60440396
geneview	rs60440396
scholar	rs60440396
google	rs60440396
pharmgkb	rs60440396
gwascentral	rs60440396
openSNP	rs60440396
23andMe	rs60440396
SNPshot	rs60440396
SNPdbe	rs60440396
MSV3d	rs60440396
GWAS Ctlg	rs60440396

Max Magnitude

0

OMIM	148065
Desc
Variant	0001
Related	also

ClinVar
Risk	rs60440396(C;C)
Alt	rs60440396(C;C)
Reference	Rs60440396(T;T)
Significance	Pathogenic
Disease	White sponge nevus 2 not provided
Variation	info
Gene	KRT13
CLNDBN	White sponge nevus 2 not provided
Reversed	1
HGVS	NC_000017.10:g.39661447A>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000015734.22, RCV000057210.1,