rs1064794983

Orientation

minus

Stabilized

minus

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

Chromosome

17

Position

41586482

Gene

KRT14

is a	snp
is	mentioned by
dbSNP	rs1064794983
dbSNP (classic)	rs1064794983
ClinGen	rs1064794983
ebi	rs1064794983
HLI	rs1064794983
Exac	rs1064794983
Gnomad	rs1064794983
Varsome	rs1064794983
LitVar	rs1064794983
Map	rs1064794983
PheGenI	rs1064794983
Biobank	rs1064794983
1000 genomes	rs1064794983
hgdp	rs1064794983
ensembl	rs1064794983
geneview	rs1064794983
scholar	rs1064794983
google	rs1064794983
pharmgkb	rs1064794983
gwascentral	rs1064794983
openSNP	rs1064794983
23andMe	rs1064794983
SNPshot	rs1064794983
SNPdbe	rs1064794983
MSV3d	rs1064794983
GWAS Ctlg	rs1064794983

Max Magnitude

0

ClinVar
Risk	rs1064794983(T;T)
Alt	rs1064794983(T;T)
Reference	Rs1064794983(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	KRT14
CLNDBN	not provided
Reversed	1
HGVS	NC_000017.10:g.39742734G>A
CLNSRC
CLNACC	RCV000487128.1,