rs1036819
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common on affy axiom data |
| Make rs1036819(A;C) |
| Make rs1036819(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 8 |
| Position | 134599702 |
| Gene | ZFAT, ZFAT-AS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1036819 |
| dbSNP (classic) | rs1036819 |
| ClinGen | rs1036819 |
| ebi | rs1036819 |
| HLI | rs1036819 |
| Exac | rs1036819 |
| Gnomad | rs1036819 |
| Varsome | rs1036819 |
| LitVar | rs1036819 |
| Map | rs1036819 |
| PheGenI | rs1036819 |
| Biobank | rs1036819 |
| 1000 genomes | rs1036819 |
| hgdp | rs1036819 |
| ensembl | rs1036819 |
| geneview | rs1036819 |
| scholar | rs1036819 |
| rs1036819 | |
| pharmgkb | rs1036819 |
| gwascentral | rs1036819 |
| openSNP | rs1036819 |
| 23andMe | rs1036819 |
| SNPshot | rs1036819 |
| SNPdbe | rs1036819 |
| MSV3d | rs1036819 |
| GWAS Ctlg | rs1036819 |
| GMAF | 0.1621 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
The most significant SNP of 150 identified as relevant to exceptional longevity in 10.1126/science.1190532; the genotype statistically associated with a greater "risk" of longevity is rs1036819(C;C).
Newsweek has reported in the article The Little Flaw in the Longevity-Gene Study That Could Be a Big Problem that the associations for rs1036819 and rs1455311 may be incorrect because of a flaw in one of the chips used.
Mentioned in retracted [PMID 20595579]
[PMID 22105264
] Identification of six Loci associated with pelvic organ prolapse using genome-wide association analysis
[PMID 31270553] Identification of pelvic organ prolapse risk susceptibility gene SNP locus in Xinjiang women.
