rs547918064
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs547918064(C;C) |
Make rs547918064(C;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 15 |
Position | 100898147 |
Gene | ALDH1A3, LOC101927751 |
is a | snp |
is | mentioned by |
dbSNP | rs547918064 |
dbSNP (classic) | rs547918064 |
ClinGen | rs547918064 |
ebi | rs547918064 |
HLI | rs547918064 |
Exac | rs547918064 |
Gnomad | rs547918064 |
Varsome | rs547918064 |
LitVar | rs547918064 |
Map | rs547918064 |
PheGenI | rs547918064 |
Biobank | rs547918064 |
1000 genomes | rs547918064 |
hgdp | rs547918064 |
ensembl | rs547918064 |
geneview | rs547918064 |
scholar | rs547918064 |
rs547918064 | |
pharmgkb | rs547918064 |
gwascentral | rs547918064 |
openSNP | rs547918064 |
23andMe | rs547918064 |
SNPshot | rs547918064 |
SNPdbe | rs547918064 |
MSV3d | rs547918064 |
GWAS Ctlg | rs547918064 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs547918064(C;C) rs547918064(T;T) |
Alt | rs547918064(C;C) rs547918064(T;T) |
Reference | Rs547918064(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | LOC101927751 ALDH1A3 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000015.9:g.101438352G>A |
CLNSRC | |
CLNACC | RCV000493670.1, |