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, |