rs61759945
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs61759945(C;T) |
Make rs61759945(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31270244 |
Gene | HLA-C |
is a | snp |
is | mentioned by |
dbSNP | rs61759945 |
dbSNP (classic) | rs61759945 |
ClinGen | rs61759945 |
ebi | rs61759945 |
HLI | rs61759945 |
Exac | rs61759945 |
Gnomad | rs61759945 |
Varsome | rs61759945 |
LitVar | rs61759945 |
Map | rs61759945 |
PheGenI | rs61759945 |
Biobank | rs61759945 |
1000 genomes | rs61759945 |
hgdp | rs61759945 |
ensembl | rs61759945 |
geneview | rs61759945 |
scholar | rs61759945 |
rs61759945 | |
pharmgkb | rs61759945 |
gwascentral | rs61759945 |
openSNP | rs61759945 |
23andMe | rs61759945 |
SNPshot | rs61759945 |
SNPdbe | rs61759945 |
MSV3d | rs61759945 |
GWAS Ctlg | rs61759945 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs61759945(T;T) |
Alt | rs61759945(T;T) |
Reference | Rs61759945(C;C) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-C |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000006.11:g.31238021G>A |
CLNSRC | |
CLNACC |