rs542184779
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs542184779(A;A) |
Make rs542184779(A;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 19 |
Position | 13110210 |
Gene | TRMT1 |
is a | snp |
is | mentioned by |
dbSNP | rs542184779 |
dbSNP (classic) | rs542184779 |
ClinGen | rs542184779 |
ebi | rs542184779 |
HLI | rs542184779 |
Exac | rs542184779 |
Gnomad | rs542184779 |
Varsome | rs542184779 |
LitVar | rs542184779 |
Map | rs542184779 |
PheGenI | rs542184779 |
Biobank | rs542184779 |
1000 genomes | rs542184779 |
hgdp | rs542184779 |
ensembl | rs542184779 |
geneview | rs542184779 |
scholar | rs542184779 |
rs542184779 | |
pharmgkb | rs542184779 |
gwascentral | rs542184779 |
openSNP | rs542184779 |
23andMe | rs542184779 |
SNPshot | rs542184779 |
SNPdbe | rs542184779 |
MSV3d | rs542184779 |
GWAS Ctlg | rs542184779 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs542184779(A;A) |
Alt | rs542184779(A;A) |
Reference | Rs542184779(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | TRMT1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000019.9:g.13221024G>A |
CLNSRC | |
CLNACC | RCV000171278.1, |