rs148360332
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs148360332(C;T) |
Make rs148360332(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 14 |
Position | 77453359 |
Gene | VIPAS39 |
is a | snp |
is | mentioned by |
dbSNP | rs148360332 |
dbSNP (classic) | rs148360332 |
ClinGen | rs148360332 |
ebi | rs148360332 |
HLI | rs148360332 |
Exac | rs148360332 |
Gnomad | rs148360332 |
Varsome | rs148360332 |
LitVar | rs148360332 |
Map | rs148360332 |
PheGenI | rs148360332 |
Biobank | rs148360332 |
1000 genomes | rs148360332 |
hgdp | rs148360332 |
ensembl | rs148360332 |
geneview | rs148360332 |
scholar | rs148360332 |
rs148360332 | |
pharmgkb | rs148360332 |
gwascentral | rs148360332 |
openSNP | rs148360332 |
23andMe | rs148360332 |
SNPshot | rs148360332 |
SNPdbe | rs148360332 |
MSV3d | rs148360332 |
GWAS Ctlg | rs148360332 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs148360332(T;T) |
Alt | rs148360332(T;T) |
Reference | Rs148360332(C;C) |
Significance | Other |
Disease | not specified |
Variation | info |
Gene | VIPAS39 |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000014.8:g.77919702C>T |
CLNSRC | |
CLNACC | RCV000171225.3, |