rs61759957
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs61759957(G;T) |
Make rs61759957(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 29942900 |
Gene | HLA-A |
is a | snp |
is | mentioned by |
dbSNP | rs61759957 |
dbSNP (classic) | rs61759957 |
ClinGen | rs61759957 |
ebi | rs61759957 |
HLI | rs61759957 |
Exac | rs61759957 |
Gnomad | rs61759957 |
Varsome | rs61759957 |
LitVar | rs61759957 |
Map | rs61759957 |
PheGenI | rs61759957 |
Biobank | rs61759957 |
1000 genomes | rs61759957 |
hgdp | rs61759957 |
ensembl | rs61759957 |
geneview | rs61759957 |
scholar | rs61759957 |
rs61759957 | |
pharmgkb | rs61759957 |
gwascentral | rs61759957 |
openSNP | rs61759957 |
23andMe | rs61759957 |
SNPshot | rs61759957 |
SNPdbe | rs61759957 |
MSV3d | rs61759957 |
GWAS Ctlg | rs61759957 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs61759957(T;T) |
Alt | rs61759957(T;T) |
Reference | Rs61759957(G;G) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-A |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000006.11:g.29910677G>T |
CLNSRC | |
CLNACC |