rs4148217
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs4148217(A;A) |
Make rs4148217(A;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 43872294 |
Gene | ABCG8 |
is a | snp |
is | mentioned by |
dbSNP | rs4148217 |
dbSNP (classic) | rs4148217 |
ClinGen | rs4148217 |
ebi | rs4148217 |
HLI | rs4148217 |
Exac | rs4148217 |
Gnomad | rs4148217 |
Varsome | rs4148217 |
LitVar | rs4148217 |
Map | rs4148217 |
PheGenI | rs4148217 |
Biobank | rs4148217 |
1000 genomes | rs4148217 |
hgdp | rs4148217 |
ensembl | rs4148217 |
geneview | rs4148217 |
scholar | rs4148217 |
rs4148217 | |
pharmgkb | rs4148217 |
gwascentral | rs4148217 |
openSNP | rs4148217 |
23andMe | rs4148217 |
SNPshot | rs4148217 |
SNPdbe | rs4148217 |
MSV3d | rs4148217 |
GWAS Ctlg | rs4148217 |
GMAF | 0.2181 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
[PMID 21062971] Cholesterol Metabolism Gene Polymorphisms and the Risk of Biliary Tract Cancers and Stones: A Population-Based Case-Control Study in Shanghai, China
[PMID 22548731] Association of ATP binding cassette transporter G8 rs4148217 SNP and serum lipid levels in Mulao and Han nationalities
[PMID 15996216] Sitosterolaemia in Switzerland: molecular genetics links the US Amish-Mennonites to their European roots.
[PMID 18778477] Genomic variation in myeloma: design, content, and initial application of the Bank On A Cure SNP Panel to detect associations with progression-free survival.
[PMID 19005228] The effects of ABCG5/G8 polymorphisms on plasma HDL cholesterol concentrations depend on smoking habit in the Boston Puerto Rican Health Study.
ClinVar | |
---|---|
Risk | rs4148217(A;A) rs4148217(T;T) |
Alt | rs4148217(A;A) rs4148217(T;T) |
Reference | Rs4148217(C;C) |
Significance | Non-pathogenic |
Disease | not specified Sitosterolemia |
Variation | info |
Gene | ABCG8 |
CLNDBN | not specified Sitosterolemia |
Reversed | 0 |
HGVS | NC_000002.11:g.44099433C>A |
CLNSRC | UniProtKB (protein) |
CLNACC | RCV000180363.1, RCV000289049.1, |
[PMID 32647408] Association of Common Single Nucleotide Polymorphisms of Candidate Genes with Gallstone Disease: A Meta-Analysis.