rs148597698
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs148597698(A;A) |
Make rs148597698(A;C) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 17 |
Position | 47945914 |
Gene | PNPO |
is a | snp |
is | mentioned by |
dbSNP | rs148597698 |
dbSNP (classic) | rs148597698 |
ClinGen | rs148597698 |
ebi | rs148597698 |
HLI | rs148597698 |
Exac | rs148597698 |
Gnomad | rs148597698 |
Varsome | rs148597698 |
LitVar | rs148597698 |
Map | rs148597698 |
PheGenI | rs148597698 |
Biobank | rs148597698 |
1000 genomes | rs148597698 |
hgdp | rs148597698 |
ensembl | rs148597698 |
geneview | rs148597698 |
scholar | rs148597698 |
rs148597698 | |
pharmgkb | rs148597698 |
gwascentral | rs148597698 |
openSNP | rs148597698 |
23andMe | rs148597698 |
SNPshot | rs148597698 |
SNPdbe | rs148597698 |
MSV3d | rs148597698 |
GWAS Ctlg | rs148597698 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs148597698(A;A) |
Alt | rs148597698(A;A) |
Reference | Rs148597698(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | PNPO |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000017.10:g.46023280C>A |
CLNSRC | |
CLNACC | RCV000188490.1, |