rs146027425
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs146027425(C;T) |
Make rs146027425(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 17 |
Position | 47945924 |
Gene | PNPO |
is a | snp |
is | mentioned by |
dbSNP | rs146027425 |
dbSNP (classic) | rs146027425 |
ClinGen | rs146027425 |
ebi | rs146027425 |
HLI | rs146027425 |
Exac | rs146027425 |
Gnomad | rs146027425 |
Varsome | rs146027425 |
LitVar | rs146027425 |
Map | rs146027425 |
PheGenI | rs146027425 |
Biobank | rs146027425 |
1000 genomes | rs146027425 |
hgdp | rs146027425 |
ensembl | rs146027425 |
geneview | rs146027425 |
scholar | rs146027425 |
rs146027425 | |
pharmgkb | rs146027425 |
gwascentral | rs146027425 |
openSNP | rs146027425 |
23andMe | rs146027425 |
SNPshot | rs146027425 |
SNPdbe | rs146027425 |
MSV3d | rs146027425 |
GWAS Ctlg | rs146027425 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs146027425(G;G) rs146027425(T;T) |
Alt | rs146027425(G;G) rs146027425(T;T) |
Reference | Rs146027425(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | PNPO |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000017.10:g.46023290C>T |
CLNSRC | |
CLNACC | RCV000188494.2, |