rs748303093
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs748303093(C;C) |
Make rs748303093(C;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 11 |
Position | 108146356 |
Gene | ACAT1 |
is a | snp |
is | mentioned by |
dbSNP | rs748303093 |
dbSNP (classic) | rs748303093 |
ClinGen | rs748303093 |
ebi | rs748303093 |
HLI | rs748303093 |
Exac | rs748303093 |
Gnomad | rs748303093 |
Varsome | rs748303093 |
LitVar | rs748303093 |
Map | rs748303093 |
PheGenI | rs748303093 |
Biobank | rs748303093 |
1000 genomes | rs748303093 |
hgdp | rs748303093 |
ensembl | rs748303093 |
geneview | rs748303093 |
scholar | rs748303093 |
rs748303093 | |
pharmgkb | rs748303093 |
gwascentral | rs748303093 |
openSNP | rs748303093 |
23andMe | rs748303093 |
SNPshot | rs748303093 |
SNPdbe | rs748303093 |
MSV3d | rs748303093 |
GWAS Ctlg | rs748303093 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs748303093(A;A) rs748303093(C;C) |
Alt | rs748303093(A;A) rs748303093(C;C) |
Reference | Rs748303093(T;T) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | ACAT1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000011.9:g.108017083T>C |
CLNSRC | |
CLNACC | RCV000493456.1, |