rs281860546
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs281860546(C;G) |
Make rs281860546(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31271085 |
Gene | HLA-C |
is a | snp |
is | mentioned by |
dbSNP | rs281860546 |
dbSNP (classic) | rs281860546 |
ClinGen | rs281860546 |
ebi | rs281860546 |
HLI | rs281860546 |
Exac | rs281860546 |
Gnomad | rs281860546 |
Varsome | rs281860546 |
LitVar | rs281860546 |
Map | rs281860546 |
PheGenI | rs281860546 |
Biobank | rs281860546 |
1000 genomes | rs281860546 |
hgdp | rs281860546 |
ensembl | rs281860546 |
geneview | rs281860546 |
scholar | rs281860546 |
rs281860546 | |
pharmgkb | rs281860546 |
gwascentral | rs281860546 |
openSNP | rs281860546 |
23andMe | rs281860546 |
SNPshot | rs281860546 |
SNPdbe | rs281860546 |
MSV3d | rs281860546 |
GWAS Ctlg | rs281860546 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs281860546(G;G) |
Alt | rs281860546(G;G) |
Reference | Rs281860546(C;C) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000006.11:g.31238862G>C |
CLNSRC | |
CLNACC |