rs387906698
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| (C;T) | 4.4 | Hereditary pancreatitis |
| Make rs387906698(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 142751919 |
| Gene | PRSS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs387906698 |
| dbSNP (classic) | rs387906698 |
| ClinGen | rs387906698 |
| ebi | rs387906698 |
| HLI | rs387906698 |
| Exac | rs387906698 |
| Gnomad | rs387906698 |
| Varsome | rs387906698 |
| LitVar | rs387906698 |
| Map | rs387906698 |
| PheGenI | rs387906698 |
| Biobank | rs387906698 |
| 1000 genomes | rs387906698 |
| hgdp | rs387906698 |
| ensembl | rs387906698 |
| geneview | rs387906698 |
| scholar | rs387906698 |
| rs387906698 | |
| pharmgkb | rs387906698 |
| gwascentral | rs387906698 |
| openSNP | rs387906698 |
| 23andMe | rs387906698 |
| SNPshot | rs387906698 |
| SNPdbe | rs387906698 |
| MSV3d | rs387906698 |
| GWAS Ctlg | rs387906698 |
| Max Magnitude | 4.4 |
aka c.346C>T, p.Arg116Cys and R116C
| ClinVar | |
|---|---|
| Risk | rs387906698(T;T) |
| Alt | rs387906698(T;T) |
| Reference | Rs387906698(C;C) |
| Significance | Pathogenic |
| Disease | Hereditary pancreatitis |
| Variation | info |
| Gene | PRSS1 |
| CLNDBN | Hereditary pancreatitis |
| Reversed | 0 |
| HGVS | NC_000007.13:g.142459770C>T |
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000022814.22, |
