rs72547570
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs72547570(A;A) |
Make rs72547570(A;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 17 |
Position | 19661163 |
Gene | ALDH3A2 |
is a | snp |
is | mentioned by |
dbSNP | rs72547570 |
dbSNP (classic) | rs72547570 |
ClinGen | rs72547570 |
ebi | rs72547570 |
HLI | rs72547570 |
Exac | rs72547570 |
Gnomad | rs72547570 |
Varsome | rs72547570 |
LitVar | rs72547570 |
Map | rs72547570 |
PheGenI | rs72547570 |
Biobank | rs72547570 |
1000 genomes | rs72547570 |
hgdp | rs72547570 |
ensembl | rs72547570 |
geneview | rs72547570 |
scholar | rs72547570 |
rs72547570 | |
pharmgkb | rs72547570 |
gwascentral | rs72547570 |
openSNP | rs72547570 |
23andMe | rs72547570 |
SNPshot | rs72547570 |
SNPdbe | rs72547570 |
MSV3d | rs72547570 |
GWAS Ctlg | rs72547570 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs72547570(A;A) |
Alt | rs72547570(A;A) |
Reference | Rs72547570(T;T) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | ALDH3A2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000017.10:g.19564476T>A |
CLNSRC | |
CLNACC | RCV000492791.1, |