rs139850307
From SNPedia
Merged into | rs1050556 |
Orientation | minus |
Stabilized | plus |
Make rs139850307(C;C) |
Make rs139850307(C;G) |
Make rs139850307(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31356809 |
Gene | HLA-B |
is a | snp |
is | mentioned by |
dbSNP | rs139850307 |
dbSNP (classic) | rs139850307 |
ClinGen | rs139850307 |
ebi | rs139850307 |
HLI | rs139850307 |
Exac | rs139850307 |
Gnomad | rs139850307 |
Varsome | rs139850307 |
LitVar | rs139850307 |
Map | rs139850307 |
PheGenI | rs139850307 |
Biobank | rs139850307 |
1000 genomes | rs139850307 |
hgdp | rs139850307 |
ensembl | rs139850307 |
geneview | rs139850307 |
scholar | rs139850307 |
rs139850307 | |
pharmgkb | rs139850307 |
gwascentral | rs139850307 |
openSNP | rs139850307 |
23andMe | rs139850307 |
SNPshot | rs139850307 |
SNPdbe | rs139850307 |
MSV3d | rs139850307 |
GWAS Ctlg | rs139850307 |
Status | Merged into rs1050556 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs139850307(T;T) |
Alt | rs139850307(T;T) |
Reference | rs139850307(C;C) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-B |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000006.11:g.31324586C>T |
CLNSRC | |
CLNACC |