rs58949162

Orientation

minus

Stabilized

minus

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

Make rs58949162(G;T)

Make rs58949162(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

12

Position

52676316

Gene

KRT1

is a	snp
is	mentioned by
dbSNP	rs58949162
dbSNP (classic)	rs58949162
ClinGen	rs58949162
ebi	rs58949162
HLI	rs58949162
Exac	rs58949162
Gnomad	rs58949162
Varsome	rs58949162
LitVar	rs58949162
Map	rs58949162
PheGenI	rs58949162
Biobank	rs58949162
1000 genomes	rs58949162
hgdp	rs58949162
ensembl	rs58949162
geneview	rs58949162
scholar	rs58949162
google	rs58949162
pharmgkb	rs58949162
gwascentral	rs58949162
openSNP	rs58949162
23andMe	rs58949162
SNPshot	rs58949162
SNPdbe	rs58949162
MSV3d	rs58949162
GWAS Ctlg	rs58949162

Max Magnitude

0

ClinVar
Risk	rs58949162(C;C) rs58949162(T;T)
Alt	rs58949162(C;C) rs58949162(T;T)
Reference	Rs58949162(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KRT1
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.53070100C>A; NC_000012.11:g.53070100C>G
CLNSRC
CLNACC	RCV000057061.1, RCV000444525.1,