rs796052033
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs796052033(A;A) |
Make rs796052033(A;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 5 |
Position | 132384263 |
Gene | SLC22A5 |
is a | snp |
is | mentioned by |
dbSNP | rs796052033 |
dbSNP (classic) | rs796052033 |
ClinGen | rs796052033 |
ebi | rs796052033 |
HLI | rs796052033 |
Exac | rs796052033 |
Gnomad | rs796052033 |
Varsome | rs796052033 |
LitVar | rs796052033 |
Map | rs796052033 |
PheGenI | rs796052033 |
Biobank | rs796052033 |
1000 genomes | rs796052033 |
hgdp | rs796052033 |
ensembl | rs796052033 |
geneview | rs796052033 |
scholar | rs796052033 |
rs796052033 | |
pharmgkb | rs796052033 |
gwascentral | rs796052033 |
openSNP | rs796052033 |
23andMe | rs796052033 |
SNPshot | rs796052033 |
SNPdbe | rs796052033 |
MSV3d | rs796052033 |
GWAS Ctlg | rs796052033 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs796052033(A;A) |
Alt | rs796052033(A;A) |
Reference | Rs796052033(T;T) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | SLC22A5 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000005.9:g.131719955T>A |
CLNSRC | |
CLNACC | RCV000186135.1, |