rs151341100
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs151341100(A;A) |
Make rs151341100(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31271824 |
Gene | HLA-C |
is a | snp |
is | mentioned by |
dbSNP | rs151341100 |
dbSNP (classic) | rs151341100 |
ClinGen | rs151341100 |
ebi | rs151341100 |
HLI | rs151341100 |
Exac | rs151341100 |
Gnomad | rs151341100 |
Varsome | rs151341100 |
LitVar | rs151341100 |
Map | rs151341100 |
PheGenI | rs151341100 |
Biobank | rs151341100 |
1000 genomes | rs151341100 |
hgdp | rs151341100 |
ensembl | rs151341100 |
geneview | rs151341100 |
scholar | rs151341100 |
rs151341100 | |
pharmgkb | rs151341100 |
gwascentral | rs151341100 |
openSNP | rs151341100 |
23andMe | rs151341100 |
SNPshot | rs151341100 |
SNPdbe | rs151341100 |
MSV3d | rs151341100 |
GWAS Ctlg | rs151341100 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs151341100(A;A) |
Alt | rs151341100(A;A) |
Reference | Rs151341100(G;G) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-B |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000006.11:g.31324690C>T |
CLNSRC | |
CLNACC |