rs63749998
From SNPedia
					| Orientation | minus | 
| Stabilized | minus | 
| Geno | Mag | Summary | 
|---|---|---|
| (T;T) | 0 | common in clinvar | 
| Make rs63749998(C;C) | 
| Make rs63749998(C;T) | 
| Reference | GRCh38 38.1/141 | 
| Chromosome | 16 | 
| Position | 16163119 | 
| Gene | ABCC6 | 
| is a | snp | 
| is | mentioned by | 
| dbSNP | rs63749998 | 
| dbSNP (classic) | rs63749998 | 
| ClinGen | rs63749998 | 
| ebi | rs63749998 | 
| HLI | rs63749998 | 
| Exac | rs63749998 | 
| Gnomad | rs63749998 | 
| Varsome | rs63749998 | 
| LitVar | rs63749998 | 
| Map | rs63749998 | 
| PheGenI | rs63749998 | 
| Biobank | rs63749998 | 
| 1000 genomes | rs63749998 | 
| hgdp | rs63749998 | 
| ensembl | rs63749998 | 
| geneview | rs63749998 | 
| scholar | rs63749998 | 
| rs63749998 | |
| pharmgkb | rs63749998 | 
| gwascentral | rs63749998 | 
| openSNP | rs63749998 | 
| 23andMe | rs63749998 | 
| SNPshot | rs63749998 | 
| SNPdbe | rs63749998 | 
| MSV3d | rs63749998 | 
| GWAS Ctlg | rs63749998 | 
| Max Magnitude | 0 | 
| ClinVar | |
|---|---|
| Risk | rs63749998(C;C) | 
| Alt | rs63749998(C;C) | 
| Reference | Rs63749998(T;T) | 
| Significance | Untested | 
| Disease | |
| Variation | info | 
| Gene | ABCC6 | 
| CLNDBN | |
| Reversed | 1 | 
| HGVS | NC_000016.9:g.16256976A>G | 
| CLNSRC | |
| CLNACC | |
