rs9264606

Orientation

plus

Stabilized

plus

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

Make rs9264606(A;C)

Make rs9264606(C;C)

Reference

GRCh38 38.1/141

Chromosome

6

Position

31269815

Gene

HLA-C

is a	snp
is	mentioned by
dbSNP	rs9264606
dbSNP (classic)	rs9264606
ClinGen	rs9264606
ebi	rs9264606
HLI	rs9264606
Exac	rs9264606
Gnomad	rs9264606
Varsome	rs9264606
LitVar	rs9264606
Map	rs9264606
PheGenI	rs9264606
Biobank	rs9264606
1000 genomes	rs9264606
hgdp	rs9264606
ensembl	rs9264606
geneview	rs9264606
scholar	rs9264606
google	rs9264606
pharmgkb	rs9264606
gwascentral	rs9264606
openSNP	rs9264606
23andMe	rs9264606
SNPshot	rs9264606
SNPdbe	rs9264606
MSV3d	rs9264606
GWAS Ctlg	rs9264606

GMAF

0.2231

Max Magnitude

0

?	(A;A) (A;C) (C;C)	28

ClinVar
Risk	rs9264606(C;C)
Alt	rs9264606(C;C)
Reference	Rs9264606(A;A)
Significance	Histocompatibility
Disease
Variation	info
Gene	HLA-C
CLNDBN
Reversed	0
HGVS	NC_000006.11:g.31237592A>C
CLNSRC
CLNACC