rs4531631
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4531631(A;A) |
| Make rs4531631(A;G) |
| Make rs4531631(G;G) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 13 |
| Position | 42560995 |
| Gene | TNFSF11 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4531631 |
| dbSNP (classic) | rs4531631 |
| ClinGen | rs4531631 |
| ebi | rs4531631 |
| HLI | rs4531631 |
| Exac | rs4531631 |
| Gnomad | rs4531631 |
| Varsome | rs4531631 |
| LitVar | rs4531631 |
| Map | rs4531631 |
| PheGenI | rs4531631 |
| Biobank | rs4531631 |
| 1000 genomes | rs4531631 |
| hgdp | rs4531631 |
| ensembl | rs4531631 |
| geneview | rs4531631 |
| scholar | rs4531631 |
| rs4531631 | |
| pharmgkb | rs4531631 |
| gwascentral | rs4531631 |
| openSNP | rs4531631 |
| 23andMe | rs4531631 |
| SNPshot | rs4531631 |
| SNPdbe | rs4531631 |
| MSV3d | rs4531631 |
| GWAS Ctlg | rs4531631 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
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| ||
[PMID 27567908] Association Between Single Nucleotide Polymorphisms in NFATC1 Signaling Pathway Genes and Susceptibility to Congenital Heart Disease in the Chinese Population.
[PMID 33058301] USF3 modulates osteoporosis risk by targeting WNT16, RANKL, RUNX2 and two GWAS lead SNPs rs2908007 and rs4531631.
