rs397514644
From SNPedia
					| Orientation | minus | 
| Stabilized | minus | 
| Geno | Mag | Summary | 
|---|---|---|
| (C;C) | 0 | common in clinvar | 
| Make rs397514644(C;T) | 
| Make rs397514644(T;T) | 
| Reference | GRCh38 38.1/141 | 
| Chromosome | 14 | 
| Position | 104780190 | 
| Gene | AKT1 | 
| is a | snp | 
| is | mentioned by | 
| dbSNP | rs397514644 | 
| dbSNP (classic) | rs397514644 | 
| ClinGen | rs397514644 | 
| ebi | rs397514644 | 
| HLI | rs397514644 | 
| Exac | rs397514644 | 
| Gnomad | rs397514644 | 
| Varsome | rs397514644 | 
| LitVar | rs397514644 | 
| Map | rs397514644 | 
| PheGenI | rs397514644 | 
| Biobank | rs397514644 | 
| 1000 genomes | rs397514644 | 
| hgdp | rs397514644 | 
| ensembl | rs397514644 | 
| geneview | rs397514644 | 
| scholar | rs397514644 | 
| rs397514644 | |
| pharmgkb | rs397514644 | 
| gwascentral | rs397514644 | 
| openSNP | rs397514644 | 
| 23andMe | rs397514644 | 
| SNPshot | rs397514644 | 
| SNPdbe | rs397514644 | 
| MSV3d | rs397514644 | 
| GWAS Ctlg | rs397514644 | 
| Max Magnitude | 0 | 
| ClinVar | |
|---|---|
| Risk | rs397514644(T;T) | 
| Alt | rs397514644(T;T) | 
| Reference | Rs397514644(C;C) | 
| Significance | Pathogenic | 
| Disease | Cowden syndrome 6 | 
| Variation | info | 
| Gene | AKT1 | 
| CLNDBN | Cowden syndrome 6 | 
| Reversed | 1 | 
| HGVS | NC_000014.8:g.105246527G>A | 
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) | 
| CLNACC | RCV000033177.26, | 
