rs9264665

Orientation

plus

Stabilized

plus

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

Make rs9264665(C;C)

Make rs9264665(C;T)

Reference

GRCh38 38.1/141

Chromosome

6

Position

31271502

Gene

HLA-C

is a	snp
is	mentioned by
dbSNP	rs9264665
dbSNP (classic)	rs9264665
ClinGen	rs9264665
ebi	rs9264665
HLI	rs9264665
Exac	rs9264665
Gnomad	rs9264665
Varsome	rs9264665
LitVar	rs9264665
Map	rs9264665
PheGenI	rs9264665
Biobank	rs9264665
1000 genomes	rs9264665
hgdp	rs9264665
ensembl	rs9264665
geneview	rs9264665
scholar	rs9264665
google	rs9264665
pharmgkb	rs9264665
gwascentral	rs9264665
openSNP	rs9264665
23andMe	rs9264665
SNPshot	rs9264665
SNPdbe	rs9264665
MSV3d	rs9264665
GWAS Ctlg	rs9264665

Max Magnitude

0

ClinVar
Risk	rs9264665(C;C)
Alt	rs9264665(C;C)
Reference	Rs9264665(T;T)
Significance	Histocompatibility
Disease
Variation	info
Gene	HLA-C
CLNDBN
Reversed	0
HGVS	NC_000006.11:g.31239279T>C
CLNSRC
CLNACC