rs3176007

Orientation

minus

Stabilized

minus

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

Make rs3176007(C;C)

Make rs3176007(C;T)

Reference

GRCh38 38.1/141

Chromosome

6

Position

31269068

Gene

HLA-C

is a	snp
is	mentioned by
dbSNP	rs3176007
dbSNP (classic)	rs3176007
ClinGen	rs3176007
ebi	rs3176007
HLI	rs3176007
Exac	rs3176007
Gnomad	rs3176007
Varsome	rs3176007
LitVar	rs3176007
Map	rs3176007
PheGenI	rs3176007
Biobank	rs3176007
1000 genomes	rs3176007
hgdp	rs3176007
ensembl	rs3176007
geneview	rs3176007
scholar	rs3176007
google	rs3176007
pharmgkb	rs3176007
gwascentral	rs3176007
openSNP	rs3176007
23andMe	rs3176007
SNPshot	rs3176007
SNPdbe	rs3176007
MSV3d	rs3176007
GWAS Ctlg	rs3176007

GMAF

0.04913

Max Magnitude

0

ClinVar
Risk	rs3176007(C;C)
Alt	rs3176007(C;C)
Reference	Rs3176007(T;T)
Significance	Histocompatibility
Disease
Variation	info
Gene	HLA-C
CLNDBN
Reversed	1
HGVS	NC_000006.11:g.31236845A>G
CLNSRC
CLNACC