rs7076156
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 2 | |
| (G;G) | 0 |
| Make rs7076156(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 10 |
| Position | 62655424 |
| Gene | LOC105378327, ZNF365 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7076156 |
| dbSNP (classic) | rs7076156 |
| ClinGen | rs7076156 |
| ebi | rs7076156 |
| HLI | rs7076156 |
| Exac | rs7076156 |
| Gnomad | rs7076156 |
| Varsome | rs7076156 |
| LitVar | rs7076156 |
| Map | rs7076156 |
| PheGenI | rs7076156 |
| Biobank | rs7076156 |
| 1000 genomes | rs7076156 |
| hgdp | rs7076156 |
| ensembl | rs7076156 |
| geneview | rs7076156 |
| scholar | rs7076156 |
| rs7076156 | |
| pharmgkb | rs7076156 |
| gwascentral | rs7076156 |
| openSNP | rs7076156 |
| 23andMe | rs7076156 |
| SNPshot | rs7076156 |
| SNPdbe | rs7076156 |
| MSV3d | rs7076156 |
| GWAS Ctlg | rs7076156 |
| GMAF | 0.152 |
| Max Magnitude | 2 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 21257989
] Variants in ZNF365 isoform D are associated with Crohn's disease
| GWAS snp | |
|---|---|
| PMID | [PMID 22412388]
|
| Trait | |
| Title | A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci. |
| Risk Allele | G |
| P-val | 7E-9 |
| Odds Ratio | 1.1900 None |
| ClinVar | |
|---|---|
| Risk | Rs7076156(G;G) |
| Alt | Rs7076156(G;G) |
| Reference | Rs7076156(A;A) |
| Significance | Other |
| Disease | Uric acid nephrolithiasis |
| Variation | info |
| Gene | ZNF365 |
| CLNDBN | Uric acid nephrolithiasis, susceptibility to |
| Reversed | 0 |
| HGVS | NC_000010.10:g.64415184A\x3d |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000002951.2, |
