rs6108011
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs6108011(C;T) |
| Make rs6108011(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 20 |
| Position | 7571857 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6108011 |
| dbSNP (classic) | rs6108011 |
| ClinGen | rs6108011 |
| ebi | rs6108011 |
| HLI | rs6108011 |
| Exac | rs6108011 |
| Gnomad | rs6108011 |
| Varsome | rs6108011 |
| LitVar | rs6108011 |
| Map | rs6108011 |
| PheGenI | rs6108011 |
| Biobank | rs6108011 |
| 1000 genomes | rs6108011 |
| hgdp | rs6108011 |
| ensembl | rs6108011 |
| geneview | rs6108011 |
| scholar | rs6108011 |
| rs6108011 | |
| pharmgkb | rs6108011 |
| gwascentral | rs6108011 |
| openSNP | rs6108011 |
| 23andMe | rs6108011 |
| SNPshot | rs6108011 |
| SNPdbe | rs6108011 |
| MSV3d | rs6108011 |
| GWAS Ctlg | rs6108011 |
| GMAF | 0.2594 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 17903294 ]
|
| Trait | Hemostatic factors and hematological phenotypes |
| Title | Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study |
| Risk Allele | |
| P-val | 0.0000060000000000000002 |
| Odds Ratio | NR NR |
[PMID 17186469] Mutations in the gene encoding the Wnt-signaling component R-spondin 4 (RSPO4) cause autosomal recessive anonychia.
