rs34505188
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common on affy axiom data |
| Make rs34505188(A;A) |
| Make rs34505188(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 227263852 |
| Gene | COL4A3, LOC654841 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs34505188 |
| dbSNP (classic) | rs34505188 |
| ClinGen | rs34505188 |
| ebi | rs34505188 |
| HLI | rs34505188 |
| Exac | rs34505188 |
| Gnomad | rs34505188 |
| Varsome | rs34505188 |
| LitVar | rs34505188 |
| Map | rs34505188 |
| PheGenI | rs34505188 |
| Biobank | rs34505188 |
| 1000 genomes | rs34505188 |
| hgdp | rs34505188 |
| ensembl | rs34505188 |
| geneview | rs34505188 |
| scholar | rs34505188 |
| rs34505188 | |
| pharmgkb | rs34505188 |
| gwascentral | rs34505188 |
| openSNP | rs34505188 |
| 23andMe | rs34505188 |
| SNPshot | rs34505188 |
| SNPdbe | rs34505188 |
| MSV3d | rs34505188 |
| GWAS Ctlg | rs34505188 |
| GMAF | 0.09642 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs34505188(A;A) |
| Alt | rs34505188(A;A) |
| Reference | Rs34505188(G;G) |
| Significance | Probable-non-pathogenic |
| Disease | not specified Alport syndrome |
| Variation | info |
| Gene | COL4A3 LOC654841 |
| CLNDBN | not specified Alport syndrome |
| Reversed | 0 |
| HGVS | NC_000002.11:g.228128568G>A |
| CLNSRC | |
| CLNACC | RCV000249936.1, RCV000267017.1, |
