rs200002200
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs200002200(A;A) |
| Make rs200002200(A;G) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 1 |
| Position | 152308777 |
| Gene | FLG |
| is a | snp |
| is | mentioned by |
| dbSNP | rs200002200 |
| dbSNP (classic) | rs200002200 |
| ClinGen | rs200002200 |
| ebi | rs200002200 |
| HLI | rs200002200 |
| Exac | rs200002200 |
| Gnomad | rs200002200 |
| Varsome | rs200002200 |
| LitVar | rs200002200 |
| Map | rs200002200 |
| PheGenI | rs200002200 |
| Biobank | rs200002200 |
| 1000 genomes | rs200002200 |
| hgdp | rs200002200 |
| ensembl | rs200002200 |
| geneview | rs200002200 |
| scholar | rs200002200 |
| rs200002200 | |
| pharmgkb | rs200002200 |
| gwascentral | rs200002200 |
| openSNP | rs200002200 |
| 23andMe | rs200002200 |
| SNPshot | rs200002200 |
| SNPdbe | rs200002200 |
| MSV3d | rs200002200 |
| GWAS Ctlg | rs200002200 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs200002200(A;A) |
| Alt | rs200002200(A;A) |
| Reference | Rs200002200(G;G) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | FLG |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000001.10:g.152281253G>A |
| CLNSRC | |
| CLNACC | RCV000261767.2, |
