rs114149656
From SNPedia
					| Orientation | plus | 
| Stabilized | plus | 
| Geno | Mag | Summary | 
|---|---|---|
| (C;C) | 0 | common in clinvar | 
| Make rs114149656(C;T) | 
| Make rs114149656(T;T) | 
| Reference | GRCh38.p7 38.3/150 | 
| Chromosome | 16 | 
| Position | 16188935 | 
| Gene | ABCC6 | 
| is a | snp | 
| is | mentioned by | 
| dbSNP | rs114149656 | 
| dbSNP (classic) | rs114149656 | 
| ClinGen | rs114149656 | 
| ebi | rs114149656 | 
| HLI | rs114149656 | 
| Exac | rs114149656 | 
| Gnomad | rs114149656 | 
| Varsome | rs114149656 | 
| LitVar | rs114149656 | 
| Map | rs114149656 | 
| PheGenI | rs114149656 | 
| Biobank | rs114149656 | 
| 1000 genomes | rs114149656 | 
| hgdp | rs114149656 | 
| ensembl | rs114149656 | 
| geneview | rs114149656 | 
| scholar | rs114149656 | 
| rs114149656 | |
| pharmgkb | rs114149656 | 
| gwascentral | rs114149656 | 
| openSNP | rs114149656 | 
| 23andMe | rs114149656 | 
| SNPshot | rs114149656 | 
| SNPdbe | rs114149656 | 
| MSV3d | rs114149656 | 
| GWAS Ctlg | rs114149656 | 
| Max Magnitude | 0 | 
| ClinVar | |
|---|---|
| Risk | rs114149656(A;A) rs114149656(T;T) | 
| Alt | rs114149656(A;A) rs114149656(T;T) | 
| Reference | Rs114149656(C;C) | 
| Significance | Pathogenic | 
| Disease | not provided | 
| Variation | info | 
| Gene | ABCC6 | 
| CLNDBN | not provided | 
| Reversed | 0 | 
| HGVS | NC_000016.9:g.16282792C>A | 
| CLNSRC | |
| CLNACC | RCV000424143.1, | 
