rs61759942

Orientation

minus

Stabilized

minus

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

Make rs61759942(C;T)

Make rs61759942(T;T)

Reference

GRCh38 38.1/141

Chromosome

6

Position

31271171

Gene

HLA-C

is a	snp
is	mentioned by
dbSNP	rs61759942
dbSNP (classic)	rs61759942
ClinGen	rs61759942
ebi	rs61759942
HLI	rs61759942
Exac	rs61759942
Gnomad	rs61759942
Varsome	rs61759942
LitVar	rs61759942
Map	rs61759942
PheGenI	rs61759942
Biobank	rs61759942
1000 genomes	rs61759942
hgdp	rs61759942
ensembl	rs61759942
geneview	rs61759942
scholar	rs61759942
google	rs61759942
pharmgkb	rs61759942
gwascentral	rs61759942
openSNP	rs61759942
23andMe	rs61759942
SNPshot	rs61759942
SNPdbe	rs61759942
MSV3d	rs61759942
GWAS Ctlg	rs61759942

Max Magnitude

0

ClinVar
Risk	rs61759942(T;T)
Alt	rs61759942(T;T)
Reference	Rs61759942(C;C)
Significance	Histocompatibility
Disease
Variation	info
Gene	HLA-C
CLNDBN
Reversed	1
HGVS	NC_000006.11:g.31238948G>A
CLNSRC
CLNACC