rs775156958
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs775156958(A;A) |
| Make rs775156958(A;T) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 1 |
| Position | 17382046 |
| Gene | PADI6 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs775156958 |
| dbSNP (classic) | rs775156958 |
| ClinGen | rs775156958 |
| ebi | rs775156958 |
| HLI | rs775156958 |
| Exac | rs775156958 |
| Gnomad | rs775156958 |
| Varsome | rs775156958 |
| LitVar | rs775156958 |
| Map | rs775156958 |
| PheGenI | rs775156958 |
| Biobank | rs775156958 |
| 1000 genomes | rs775156958 |
| hgdp | rs775156958 |
| ensembl | rs775156958 |
| geneview | rs775156958 |
| scholar | rs775156958 |
| rs775156958 | |
| pharmgkb | rs775156958 |
| gwascentral | rs775156958 |
| openSNP | rs775156958 |
| 23andMe | rs775156958 |
| SNPshot | rs775156958 |
| SNPdbe | rs775156958 |
| MSV3d | rs775156958 |
| GWAS Ctlg | rs775156958 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs775156958(A;A) |
| Alt | rs775156958(A;A) |
| Reference | Rs775156958(T;T) |
| Significance | Pathogenic |
| Disease | Preimplantation embryonic lethality 2 |
| Variation | info |
| Gene | PADI6 |
| CLNDBN | Preimplantation embryonic lethality 2 |
| Reversed | 0 |
| HGVS | NC_000001.10:g.17708541T>A |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000412664.1, |
