rs372753711
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs372753711(A;A) |
Make rs372753711(A;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 12 |
Position | 131939188 |
Gene | PUS1 |
is a | snp |
is | mentioned by |
dbSNP | rs372753711 |
dbSNP (classic) | rs372753711 |
ClinGen | rs372753711 |
ebi | rs372753711 |
HLI | rs372753711 |
Exac | rs372753711 |
Gnomad | rs372753711 |
Varsome | rs372753711 |
LitVar | rs372753711 |
Map | rs372753711 |
PheGenI | rs372753711 |
Biobank | rs372753711 |
1000 genomes | rs372753711 |
hgdp | rs372753711 |
ensembl | rs372753711 |
geneview | rs372753711 |
scholar | rs372753711 |
rs372753711 | |
pharmgkb | rs372753711 |
gwascentral | rs372753711 |
openSNP | rs372753711 |
23andMe | rs372753711 |
SNPshot | rs372753711 |
SNPdbe | rs372753711 |
MSV3d | rs372753711 |
GWAS Ctlg | rs372753711 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs372753711(A;A) |
Alt | rs372753711(A;A) |
Reference | Rs372753711(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | PUS1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000012.11:g.132423733G>A |
CLNSRC | |
CLNACC | RCV000199180.1, |