rs267607448

Orientation

minus

Stabilized

minus

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

Make rs267607448(C;T)

Make rs267607448(T;T)

Reference

GRCh38.p7 38.3/149

Chromosome

12

Position

52516665

Gene

KRT5

is a	snp
is	mentioned by
dbSNP	rs267607448
dbSNP (classic)	rs267607448
ClinGen	rs267607448
ebi	rs267607448
HLI	rs267607448
Exac	rs267607448
Gnomad	rs267607448
Varsome	rs267607448
LitVar	rs267607448
Map	rs267607448
PheGenI	rs267607448
Biobank	rs267607448
1000 genomes	rs267607448
hgdp	rs267607448
ensembl	rs267607448
geneview	rs267607448
scholar	rs267607448
google	rs267607448
pharmgkb	rs267607448
gwascentral	rs267607448
openSNP	rs267607448
23andMe	rs267607448
SNPshot	rs267607448
SNPdbe	rs267607448
MSV3d	rs267607448
GWAS Ctlg	rs267607448

Max Magnitude

0

ClinVar
Risk	rs267607448(T;T)
Alt	rs267607448(T;T)
Reference	Rs267607448(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KRT5
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.52910449G>A
CLNSRC
CLNACC	RCV000056559.2,