rs879253889
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs879253889(C;T) |
Make rs879253889(T;T) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 1 |
Position | 156868201 |
Gene | NTRK1 |
is a | snp |
is | mentioned by |
dbSNP | rs879253889 |
dbSNP (classic) | rs879253889 |
ClinGen | rs879253889 |
ebi | rs879253889 |
HLI | rs879253889 |
Exac | rs879253889 |
Gnomad | rs879253889 |
Varsome | rs879253889 |
LitVar | rs879253889 |
Map | rs879253889 |
PheGenI | rs879253889 |
Biobank | rs879253889 |
1000 genomes | rs879253889 |
hgdp | rs879253889 |
ensembl | rs879253889 |
geneview | rs879253889 |
scholar | rs879253889 |
rs879253889 | |
pharmgkb | rs879253889 |
gwascentral | rs879253889 |
openSNP | rs879253889 |
23andMe | rs879253889 |
SNPshot | rs879253889 |
SNPdbe | rs879253889 |
MSV3d | rs879253889 |
GWAS Ctlg | rs879253889 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs879253889(T;T) |
Alt | rs879253889(T;T) |
Reference | Rs879253889(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | NTRK1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000001.10:g.156837993C>T |
CLNSRC | |
CLNACC | RCV000236167.1, |