rs1049668

Orientation

minus

Stabilized

minus

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

Make rs1049668(A;A)

Make rs1049668(A;G)

Reference

GRCh38 38.1/141

Chromosome

6

Position

31269044

Gene

HLA-C

is a	snp
is	mentioned by
dbSNP	rs1049668
dbSNP (classic)	rs1049668
ClinGen	rs1049668
ebi	rs1049668
HLI	rs1049668
Exac	rs1049668
Gnomad	rs1049668
Varsome	rs1049668
LitVar	rs1049668
Map	rs1049668
PheGenI	rs1049668
Biobank	rs1049668
1000 genomes	rs1049668
hgdp	rs1049668
ensembl	rs1049668
geneview	rs1049668
scholar	rs1049668
google	rs1049668
pharmgkb	rs1049668
gwascentral	rs1049668
openSNP	rs1049668
23andMe	rs1049668
SNPshot	rs1049668
SNPdbe	rs1049668
MSV3d	rs1049668
GWAS Ctlg	rs1049668

GMAF

0.02571

Max Magnitude

0

ClinVar
Risk	rs1049668(A;A)
Alt	rs1049668(A;A)
Reference	Rs1049668(G;G)
Significance	Histocompatibility
Disease
Variation	info
Gene	HLA-C
CLNDBN
Reversed	1
HGVS	NC_000006.11:g.31236821C>T
CLNSRC
CLNACC