rs761848742
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs761848742(C;T) |
Make rs761848742(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 9 |
Position | 131521439 |
Gene | POMT1 |
is a | snp |
is | mentioned by |
dbSNP | rs761848742 |
dbSNP (classic) | rs761848742 |
ClinGen | rs761848742 |
ebi | rs761848742 |
HLI | rs761848742 |
Exac | rs761848742 |
Gnomad | rs761848742 |
Varsome | rs761848742 |
LitVar | rs761848742 |
Map | rs761848742 |
PheGenI | rs761848742 |
Biobank | rs761848742 |
1000 genomes | rs761848742 |
hgdp | rs761848742 |
ensembl | rs761848742 |
geneview | rs761848742 |
scholar | rs761848742 |
rs761848742 | |
pharmgkb | rs761848742 |
gwascentral | rs761848742 |
openSNP | rs761848742 |
23andMe | rs761848742 |
SNPshot | rs761848742 |
SNPdbe | rs761848742 |
MSV3d | rs761848742 |
GWAS Ctlg | rs761848742 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs761848742(T;T) |
Alt | rs761848742(T;T) |
Reference | Rs761848742(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | POMT1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000009.11:g.134396826C>T |
CLNSRC | |
CLNACC | RCV000487062.1, |