rs869025324
From SNPedia
					| Orientation | plus | 
| Stabilized | plus | 
| Make rs869025324(A;A) | 
| Make rs869025324(A;G) | 
| Reference | GRCh38.p2 38.2/147 | 
| Chromosome | 2 | 
| Position | 227253337 | 
| Gene | COL4A3, LOC654841 | 
| is a | snp | 
| is | mentioned by | 
| dbSNP | rs869025324 | 
| dbSNP (classic) | rs869025324 | 
| ClinGen | rs869025324 | 
| ebi | rs869025324 | 
| HLI | rs869025324 | 
| Exac | rs869025324 | 
| Gnomad | rs869025324 | 
| Varsome | rs869025324 | 
| LitVar | rs869025324 | 
| Map | rs869025324 | 
| PheGenI | rs869025324 | 
| Biobank | rs869025324 | 
| 1000 genomes | rs869025324 | 
| hgdp | rs869025324 | 
| ensembl | rs869025324 | 
| geneview | rs869025324 | 
| scholar | rs869025324 | 
| rs869025324 | |
| pharmgkb | rs869025324 | 
| gwascentral | rs869025324 | 
| openSNP | rs869025324 | 
| 23andMe | rs869025324 | 
| SNPshot | rs869025324 | 
| SNPdbe | rs869025324 | 
| MSV3d | rs869025324 | 
| GWAS Ctlg | rs869025324 | 
| Max Magnitude | 0 | 
| ClinVar | |
|---|---|
| Risk | rs869025324(A;A) | 
| Alt | rs869025324(A;A) | 
| Reference | Rs869025324(G;G) | 
| Significance | Pathogenic | 
| Disease | Alport syndrome | 
| Variation | info | 
| Gene | COL4A3 LOC654841 | 
| CLNDBN | Alport syndrome, autosomal recessive | 
| Reversed | 0 | 
| HGVS | NC_000002.11:g.228118053G>A | 
| CLNSRC | |
| CLNACC | RCV000207840.1, | 


