rs151341234
From SNPedia
Merged into | rs151341233 |
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs151341234(C;C) |
Make rs151341234(C;G) |
Reference | GRCh37.p5 37.3/137 |
Chromosome | 6 |
Position | 31324159 |
Gene | HLA-B |
is a | snp |
is | mentioned by |
dbSNP | rs151341234 |
dbSNP (classic) | rs151341234 |
ClinGen | rs151341234 |
ebi | rs151341234 |
HLI | rs151341234 |
Exac | rs151341234 |
Gnomad | rs151341234 |
Varsome | rs151341234 |
LitVar | rs151341234 |
Map | rs151341234 |
PheGenI | rs151341234 |
Biobank | rs151341234 |
1000 genomes | rs151341234 |
hgdp | rs151341234 |
ensembl | rs151341234 |
geneview | rs151341234 |
scholar | rs151341234 |
rs151341234 | |
pharmgkb | rs151341234 |
gwascentral | rs151341234 |
openSNP | rs151341234 |
23andMe | rs151341234 |
SNPshot | rs151341234 |
SNPdbe | rs151341234 |
MSV3d | rs151341234 |
GWAS Ctlg | rs151341234 |
Status | Merged into rs151341233 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs151341234(C;C) |
Alt | rs151341234(C;C) |
Reference | Rs151341234(G;G) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-B |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000006.11:g.31324159C>G |
CLNSRC | |
CLNACC |