rs12721717
From SNPedia
Merged into | rs1059498 |
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs12721717(C;C) |
Make rs12721717(C;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 29943338 |
Gene | HLA-A |
is a | snp |
is | mentioned by |
dbSNP | rs12721717 |
dbSNP (classic) | rs12721717 |
ClinGen | rs12721717 |
ebi | rs12721717 |
HLI | rs12721717 |
Exac | rs12721717 |
Gnomad | rs12721717 |
Varsome | rs12721717 |
LitVar | rs12721717 |
Map | rs12721717 |
PheGenI | rs12721717 |
Biobank | rs12721717 |
1000 genomes | rs12721717 |
hgdp | rs12721717 |
ensembl | rs12721717 |
geneview | rs12721717 |
scholar | rs12721717 |
rs12721717 | |
pharmgkb | rs12721717 |
gwascentral | rs12721717 |
openSNP | rs12721717 |
23andMe | rs12721717 |
SNPshot | rs12721717 |
SNPdbe | rs12721717 |
MSV3d | rs12721717 |
GWAS Ctlg | rs12721717 |
Status | Merged into rs1059498 |
GMAF | 0.432 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs12721717(A;A) rs12721717(C;C) rs12721717(T;T) |
Alt | rs12721717(A;A) rs12721717(C;C) rs12721717(T;T) |
Reference | Rs12721717(G;G) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-A |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000006.11:g.29911115G>A; NC_000006.11:g.29911115G>C; NC_000006.11:g.29911115G>T |
CLNSRC | |
CLNACC |