rs151166046
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs151166046(A;A) |
Make rs151166046(A;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 2 |
Position | 55680879 |
Gene | PNPT1 |
is a | snp |
is | mentioned by |
dbSNP | rs151166046 |
dbSNP (classic) | rs151166046 |
ClinGen | rs151166046 |
ebi | rs151166046 |
HLI | rs151166046 |
Exac | rs151166046 |
Gnomad | rs151166046 |
Varsome | rs151166046 |
LitVar | rs151166046 |
Map | rs151166046 |
PheGenI | rs151166046 |
Biobank | rs151166046 |
1000 genomes | rs151166046 |
hgdp | rs151166046 |
ensembl | rs151166046 |
geneview | rs151166046 |
scholar | rs151166046 |
rs151166046 | |
pharmgkb | rs151166046 |
gwascentral | rs151166046 |
openSNP | rs151166046 |
23andMe | rs151166046 |
SNPshot | rs151166046 |
SNPdbe | rs151166046 |
MSV3d | rs151166046 |
GWAS Ctlg | rs151166046 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs151166046(A;A) |
Alt | rs151166046(A;A) |
Reference | Rs151166046(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | PNPT1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.55908014G>A |
CLNSRC | |
CLNACC | RCV000199028.2, |