rs886039403

Orientation

minus

Stabilized

minus

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

Make rs886039403(A;A)

Make rs886039403(A;G)

Reference

GRCh38.p7 38.3/149

Chromosome

12

Position

52519741

Gene

KRT5

is a	snp
is	mentioned by
dbSNP	rs886039403
dbSNP (classic)	rs886039403
ClinGen	rs886039403
ebi	rs886039403
HLI	rs886039403
Exac	rs886039403
Gnomad	rs886039403
Varsome	rs886039403
LitVar	rs886039403
Map	rs886039403
PheGenI	rs886039403
Biobank	rs886039403
1000 genomes	rs886039403
hgdp	rs886039403
ensembl	rs886039403
geneview	rs886039403
scholar	rs886039403
google	rs886039403
pharmgkb	rs886039403
gwascentral	rs886039403
openSNP	rs886039403
23andMe	rs886039403
SNPshot	rs886039403
SNPdbe	rs886039403
MSV3d	rs886039403
GWAS Ctlg	rs886039403

Max Magnitude

0

ClinVar
Risk	rs886039403(A;A)
Alt	rs886039403(A;A)
Reference	Rs886039403(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KRT5
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.52913525C>T
CLNSRC
CLNACC	RCV000255331.1,