rs61760866
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs61760866(-;-) |
Make rs61760866(-;C) |
Reference | GRCh37.p5 37.3/137 |
Chromosome | 6 |
Position | 29910739 |
Gene | HLA-A |
is a | snp |
is | mentioned by |
dbSNP | rs61760866 |
dbSNP (classic) | rs61760866 |
ClinGen | rs61760866 |
ebi | rs61760866 |
HLI | rs61760866 |
Exac | rs61760866 |
Gnomad | rs61760866 |
Varsome | rs61760866 |
LitVar | rs61760866 |
Map | rs61760866 |
PheGenI | rs61760866 |
Biobank | rs61760866 |
1000 genomes | rs61760866 |
hgdp | rs61760866 |
ensembl | rs61760866 |
geneview | rs61760866 |
scholar | rs61760866 |
rs61760866 | |
pharmgkb | rs61760866 |
gwascentral | rs61760866 |
openSNP | rs61760866 |
23andMe | rs61760866 |
SNPshot | rs61760866 |
SNPdbe | rs61760866 |
MSV3d | rs61760866 |
GWAS Ctlg | rs61760866 |
Status | Deleted |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | |
Alt | |
Reference | Rs61760866(C;C) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-A |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000006.11:g.29910739delC |
CLNSRC | |
CLNACC |