rs149105551
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs149105551(C;C) |
| Make rs149105551(C;G) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 1 |
| Position | 152309494 |
| Gene | FLG |
| is a | snp |
| is | mentioned by |
| dbSNP | rs149105551 |
| dbSNP (classic) | rs149105551 |
| ClinGen | rs149105551 |
| ebi | rs149105551 |
| HLI | rs149105551 |
| Exac | rs149105551 |
| Gnomad | rs149105551 |
| Varsome | rs149105551 |
| LitVar | rs149105551 |
| Map | rs149105551 |
| PheGenI | rs149105551 |
| Biobank | rs149105551 |
| 1000 genomes | rs149105551 |
| hgdp | rs149105551 |
| ensembl | rs149105551 |
| geneview | rs149105551 |
| scholar | rs149105551 |
| rs149105551 | |
| pharmgkb | rs149105551 |
| gwascentral | rs149105551 |
| openSNP | rs149105551 |
| 23andMe | rs149105551 |
| SNPshot | rs149105551 |
| SNPdbe | rs149105551 |
| MSV3d | rs149105551 |
| GWAS Ctlg | rs149105551 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs149105551(A;A) rs149105551(C;C) rs149105551(T;T) |
| Alt | rs149105551(A;A) rs149105551(C;C) rs149105551(T;T) |
| Reference | Rs149105551(G;G) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | FLG |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000001.10:g.152281970G>A |
| CLNSRC | |
| CLNACC | RCV000484307.1, |
