rs281860477

Orientation

minus

Stabilized

minus

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

Make rs281860477(C;C)

Make rs281860477(C;T)

Reference

GRCh38 38.1/141

Chromosome

6

Position

31271253

Gene

HLA-C

is a	snp
is	mentioned by
dbSNP	rs281860477
dbSNP (classic)	rs281860477
ClinGen	rs281860477
ebi	rs281860477
HLI	rs281860477
Exac	rs281860477
Gnomad	rs281860477
Varsome	rs281860477
LitVar	rs281860477
Map	rs281860477
PheGenI	rs281860477
Biobank	rs281860477
1000 genomes	rs281860477
hgdp	rs281860477
ensembl	rs281860477
geneview	rs281860477
scholar	rs281860477
google	rs281860477
pharmgkb	rs281860477
gwascentral	rs281860477
openSNP	rs281860477
23andMe	rs281860477
SNPshot	rs281860477
SNPdbe	rs281860477
MSV3d	rs281860477
GWAS Ctlg	rs281860477

Max Magnitude

0

ClinVar
Risk	rs281860477(C;C)
Alt	rs281860477(C;C)
Reference	Rs281860477(T;T)
Significance	Histocompatibility
Disease
Variation	info
Gene
CLNDBN
Reversed	1
HGVS	NC_000006.11:g.31239030A>G
CLNSRC
CLNACC