rs151341293
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs151341293(-;-) |
Make rs151341293(-;A) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31356259 |
Gene | HLA-B, MIR6891 |
is a | snp |
is | mentioned by |
dbSNP | rs151341293 |
dbSNP (classic) | rs151341293 |
ClinGen | rs151341293 |
ebi | rs151341293 |
HLI | rs151341293 |
Exac | rs151341293 |
Gnomad | rs151341293 |
Varsome | rs151341293 |
LitVar | rs151341293 |
Map | rs151341293 |
PheGenI | rs151341293 |
Biobank | rs151341293 |
1000 genomes | rs151341293 |
hgdp | rs151341293 |
ensembl | rs151341293 |
geneview | rs151341293 |
scholar | rs151341293 |
rs151341293 | |
pharmgkb | rs151341293 |
gwascentral | rs151341293 |
openSNP | rs151341293 |
23andMe | rs151341293 |
SNPshot | rs151341293 |
SNPdbe | rs151341293 |
MSV3d | rs151341293 |
GWAS Ctlg | rs151341293 |
Merged from | Rs151341294 |
GMAF | 0.4091 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | |
Alt | |
Reference | Rs151341293(A;A) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-B |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000006.11:g.31324036delT |
CLNSRC | |
CLNACC |