rs267607400

Orientation

minus

Stabilized

minus

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

Make rs267607400(C;T)

Make rs267607400(T;T)

Reference

GRCh38.p7 38.3/149

Chromosome

17

Position

41583281

Gene

KRT14

is a	snp
is	mentioned by
dbSNP	rs267607400
dbSNP (classic)	rs267607400
ClinGen	rs267607400
ebi	rs267607400
HLI	rs267607400
Exac	rs267607400
Gnomad	rs267607400
Varsome	rs267607400
LitVar	rs267607400
Map	rs267607400
PheGenI	rs267607400
Biobank	rs267607400
1000 genomes	rs267607400
hgdp	rs267607400
ensembl	rs267607400
geneview	rs267607400
scholar	rs267607400
google	rs267607400
pharmgkb	rs267607400
gwascentral	rs267607400
openSNP	rs267607400
23andMe	rs267607400
SNPshot	rs267607400
SNPdbe	rs267607400
MSV3d	rs267607400
GWAS Ctlg	rs267607400

Max Magnitude

0

ClinVar
Risk	rs267607400(T;T)
Alt	rs267607400(T;T)
Reference	Rs267607400(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KRT14
CLNDBN	not provided
Reversed	1
HGVS	NC_000017.10:g.39739533G>A
CLNSRC
CLNACC	RCV000056676.2,