rs606231467
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs606231467(A;A) |
Make rs606231467(A;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 1 |
Position | 156876128 |
Gene | NTRK1 |
is a | snp |
is | mentioned by |
dbSNP | rs606231467 |
dbSNP (classic) | rs606231467 |
ClinGen | rs606231467 |
ebi | rs606231467 |
HLI | rs606231467 |
Exac | rs606231467 |
Gnomad | rs606231467 |
Varsome | rs606231467 |
LitVar | rs606231467 |
Map | rs606231467 |
PheGenI | rs606231467 |
Biobank | rs606231467 |
1000 genomes | rs606231467 |
hgdp | rs606231467 |
ensembl | rs606231467 |
geneview | rs606231467 |
scholar | rs606231467 |
rs606231467 | |
pharmgkb | rs606231467 |
gwascentral | rs606231467 |
openSNP | rs606231467 |
23andMe | rs606231467 |
SNPshot | rs606231467 |
SNPdbe | rs606231467 |
MSV3d | rs606231467 |
GWAS Ctlg | rs606231467 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs606231467(A;A) |
Alt | rs606231467(A;A) |
Reference | Rs606231467(G;G) |
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.156845920G>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000148946.3, |