rs398122810
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(TG;TG) | 0 | common in clinvar |
Make rs398122810(-;-) |
Make rs398122810(-;TG) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 156861141 |
Gene | NTRK1 |
is a | snp |
is | mentioned by |
dbSNP | rs398122810 |
dbSNP (classic) | rs398122810 |
ClinGen | rs398122810 |
ebi | rs398122810 |
HLI | rs398122810 |
Exac | rs398122810 |
Gnomad | rs398122810 |
Varsome | rs398122810 |
LitVar | rs398122810 |
Map | rs398122810 |
PheGenI | rs398122810 |
Biobank | rs398122810 |
1000 genomes | rs398122810 |
hgdp | rs398122810 |
ensembl | rs398122810 |
geneview | rs398122810 |
scholar | rs398122810 |
rs398122810 | |
pharmgkb | rs398122810 |
gwascentral | rs398122810 |
openSNP | rs398122810 |
23andMe | rs398122810 |
SNPshot | rs398122810 |
SNPdbe | rs398122810 |
MSV3d | rs398122810 |
GWAS Ctlg | rs398122810 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs398122810(-;-) |
Alt | rs398122810(-;-) |
Reference | Rs398122810(TG;TG) |
Significance | Pathogenic |
Disease | Hereditary insensitivity to pain with anhidrosis |
Variation | info |
Gene | NTRK1 |
CLNDBN | Hereditary insensitivity to pain with anhidrosis |
Reversed | 0 |
HGVS | NC_000001.10:g.156830933_156830934delTG |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000022807.18, |