rs1050366

Orientation

minus

Stabilized

minus

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

Make rs1050366(G;G)

Make rs1050366(G;T)

Reference

GRCh38 38.1/141

Chromosome

6

Position

31271180

Gene

HLA-C

is a	snp
is	mentioned by
dbSNP	rs1050366
dbSNP (classic)	rs1050366
ClinGen	rs1050366
ebi	rs1050366
HLI	rs1050366
Exac	rs1050366
Gnomad	rs1050366
Varsome	rs1050366
LitVar	rs1050366
Map	rs1050366
PheGenI	rs1050366
Biobank	rs1050366
1000 genomes	rs1050366
hgdp	rs1050366
ensembl	rs1050366
geneview	rs1050366
scholar	rs1050366
google	rs1050366
pharmgkb	rs1050366
gwascentral	rs1050366
openSNP	rs1050366
23andMe	rs1050366
SNPshot	rs1050366
SNPdbe	rs1050366
MSV3d	rs1050366
GWAS Ctlg	rs1050366

GMAF

0.3691

Max Magnitude

0

ClinVar
Risk	rs1050366(A;A) rs1050366(G;G)
Alt	rs1050366(A;A) rs1050366(G;G)
Reference	Rs1050366(T;T)
Significance	Histocompatibility
Disease
Variation	info
Gene	HLA-C
CLNDBN
Reversed	1
HGVS	NC_000006.11:g.31238957A>C; NC_000006.11:g.31238957A>T
CLNSRC
CLNACC