rs770561064
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs770561064(C;T) |
Make rs770561064(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 15 |
Position | 31076919 |
Gene | TRPM1 |
is a | snp |
is | mentioned by |
dbSNP | rs770561064 |
dbSNP (classic) | rs770561064 |
ClinGen | rs770561064 |
ebi | rs770561064 |
HLI | rs770561064 |
Exac | rs770561064 |
Gnomad | rs770561064 |
Varsome | rs770561064 |
LitVar | rs770561064 |
Map | rs770561064 |
PheGenI | rs770561064 |
Biobank | rs770561064 |
1000 genomes | rs770561064 |
hgdp | rs770561064 |
ensembl | rs770561064 |
geneview | rs770561064 |
scholar | rs770561064 |
rs770561064 | |
pharmgkb | rs770561064 |
gwascentral | rs770561064 |
openSNP | rs770561064 |
23andMe | rs770561064 |
SNPshot | rs770561064 |
SNPdbe | rs770561064 |
MSV3d | rs770561064 |
GWAS Ctlg | rs770561064 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs770561064(T;T) |
Alt | rs770561064(T;T) |
Reference | Rs770561064(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | TRPM1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000015.9:g.31369122C>T |
CLNSRC | |
CLNACC | RCV000171229.1, |