rs35669708
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs35669708(C;C) |
| Make rs35669708(C;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 156881590 |
| Gene | NTRK1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs35669708 |
| dbSNP (classic) | rs35669708 |
| ClinGen | rs35669708 |
| ebi | rs35669708 |
| HLI | rs35669708 |
| Exac | rs35669708 |
| Gnomad | rs35669708 |
| Varsome | rs35669708 |
| LitVar | rs35669708 |
| Map | rs35669708 |
| PheGenI | rs35669708 |
| Biobank | rs35669708 |
| 1000 genomes | rs35669708 |
| hgdp | rs35669708 |
| ensembl | rs35669708 |
| geneview | rs35669708 |
| scholar | rs35669708 |
| rs35669708 | |
| pharmgkb | rs35669708 |
| gwascentral | rs35669708 |
| openSNP | rs35669708 |
| 23andMe | rs35669708 |
| SNPshot | rs35669708 |
| SNPdbe | rs35669708 |
| MSV3d | rs35669708 |
| GWAS Ctlg | rs35669708 |
| GMAF | 0.003673 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs35669708(A;A) rs35669708(C;C) |
| Alt | rs35669708(A;A) rs35669708(C;C) |
| Reference | Rs35669708(G;G) |
| Significance | Pathogenic |
| Disease | not provided not specified Hereditary insensitivity to pain with anhidrosis |
| Variation | info |
| Gene | NTRK1 |
| CLNDBN | not provided not specified Hereditary insensitivity to pain with anhidrosis |
| Reversed | 0 |
| HGVS | NC_000001.10:g.156851382G>A; NC_000001.10:g.156851382G>C |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000224279.1, RCV000236228.2, RCV000013097.23, |
