rs71369530
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (GGCGGC;GGCGGC) | 0 | common in clinvar |
| Make rs71369530(-;-) |
| Make rs71369530(-;GGCGGC) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 9 |
| Position | 97854446 |
| Gene | FOXE1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs71369530 |
| dbSNP (classic) | rs71369530 |
| ClinGen | rs71369530 |
| ebi | rs71369530 |
| HLI | rs71369530 |
| Exac | rs71369530 |
| Gnomad | rs71369530 |
| Varsome | rs71369530 |
| LitVar | rs71369530 |
| Map | rs71369530 |
| PheGenI | rs71369530 |
| Biobank | rs71369530 |
| 1000 genomes | rs71369530 |
| hgdp | rs71369530 |
| ensembl | rs71369530 |
| geneview | rs71369530 |
| scholar | rs71369530 |
| rs71369530 | |
| pharmgkb | rs71369530 |
| gwascentral | rs71369530 |
| openSNP | rs71369530 |
| 23andMe | rs71369530 |
| SNPshot | rs71369530 |
| SNPdbe | rs71369530 |
| MSV3d | rs71369530 |
| GWAS Ctlg | rs71369530 |
| Max Magnitude | 0 |
[PMID 25879635
] Common variants at the 9q22.33, 14q13.3 and ATM loci, and risk of differentiated thyroid cancer in the Cuban population
| ClinVar | |
|---|---|
| Risk | rs71369530(-;-) |
| Alt | rs71369530(-;-) |
| Reference | Rs71369530(GGCGGC;GGCGGC) |
| Significance | Non-pathogenic |
| Disease | not specified |
| Variation | info |
| Gene | LOC101928337 FOXE1 |
| CLNDBN | not specified |
| Reversed | 1 |
| HGVS | NC_000009.11:g.100616728_100616733delGCCGCC |
| CLNSRC | |
| CLNACC | RCV000081102.5, |
