rs1049650

Orientation

minus

Stabilized

minus

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

Make rs1049650(C;C)

Make rs1049650(C;G)

Reference

GRCh38 38.1/141

Chromosome

6

Position

31269031

Gene

HLA-C

is a	snp
is	mentioned by
dbSNP	rs1049650
dbSNP (classic)	rs1049650
ClinGen	rs1049650
ebi	rs1049650
HLI	rs1049650
Exac	rs1049650
Gnomad	rs1049650
Varsome	rs1049650
LitVar	rs1049650
Map	rs1049650
PheGenI	rs1049650
Biobank	rs1049650
1000 genomes	rs1049650
hgdp	rs1049650
ensembl	rs1049650
geneview	rs1049650
scholar	rs1049650
google	rs1049650
pharmgkb	rs1049650
gwascentral	rs1049650
openSNP	rs1049650
23andMe	rs1049650
SNPshot	rs1049650
SNPdbe	rs1049650
MSV3d	rs1049650
GWAS Ctlg	rs1049650

GMAF

0.1244

Max Magnitude

0

ClinVar
Risk	rs1049650(C;C)
Alt	rs1049650(C;C)
Reference	Rs1049650(G;G)
Significance	Histocompatibility
Disease
Variation	info
Gene	HLA-C
CLNDBN
Reversed	1
HGVS	NC_000006.11:g.31236808C>G
CLNSRC
CLNACC