rs60271599

Orientation

minus

Stabilized

minus

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

Make rs60271599(C;C)

Make rs60271599(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

12

Position

52516676

Gene

KRT5

is a	snp
is	mentioned by
dbSNP	rs60271599
dbSNP (classic)	rs60271599
ClinGen	rs60271599
ebi	rs60271599
HLI	rs60271599
Exac	rs60271599
Gnomad	rs60271599
Varsome	rs60271599
LitVar	rs60271599
Map	rs60271599
PheGenI	rs60271599
Biobank	rs60271599
1000 genomes	rs60271599
hgdp	rs60271599
ensembl	rs60271599
geneview	rs60271599
scholar	rs60271599
google	rs60271599
pharmgkb	rs60271599
gwascentral	rs60271599
openSNP	rs60271599
23andMe	rs60271599
SNPshot	rs60271599
SNPdbe	rs60271599
MSV3d	rs60271599
GWAS Ctlg	rs60271599

Max Magnitude

0

ClinVar
Risk	rs60271599(C;C)
Alt	rs60271599(C;C)
Reference	Rs60271599(T;T)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KRT5
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.52910460A>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000056556.1,