rs41278172
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs41278172(A;A) |
| Make rs41278172(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 16161567 |
| Gene | ABCC6 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs41278172 |
| dbSNP (classic) | rs41278172 |
| ClinGen | rs41278172 |
| ebi | rs41278172 |
| HLI | rs41278172 |
| Exac | rs41278172 |
| Gnomad | rs41278172 |
| Varsome | rs41278172 |
| LitVar | rs41278172 |
| Map | rs41278172 |
| PheGenI | rs41278172 |
| Biobank | rs41278172 |
| 1000 genomes | rs41278172 |
| hgdp | rs41278172 |
| ensembl | rs41278172 |
| geneview | rs41278172 |
| scholar | rs41278172 |
| rs41278172 | |
| pharmgkb | rs41278172 |
| gwascentral | rs41278172 |
| openSNP | rs41278172 |
| 23andMe | rs41278172 |
| SNPshot | rs41278172 |
| SNPdbe | rs41278172 |
| MSV3d | rs41278172 |
| GWAS Ctlg | rs41278172 |
| GMAF | 0.0124 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs41278172(A;A) |
| Alt | rs41278172(A;A) |
| Reference | Rs41278172(G;G) |
| Significance | Non-pathogenic |
| Disease | not specified |
| Variation | info |
| Gene | ABCC6 |
| CLNDBN | not specified |
| Reversed | 0 |
| HGVS | NC_000016.9:g.16255424G>A |
| CLNSRC | |
| CLNACC | RCV000393125.1, |
