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rs3806471

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs3806471(A;C)
Make rs3806471(C;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position43839035
GeneABCG8
is asnp
is mentioned by
dbSNPrs3806471
ebirs3806471
HLIrs3806471
Exacrs3806471
Varsomers3806471
Maprs3806471
PheGenIrs3806471
hapmaprs3806471
1000 genomesrs3806471
hgdprs3806471
ensemblrs3806471
gopubmedrs3806471
geneviewrs3806471
scholarrs3806471
googlers3806471
pharmgkbrs3806471
gwascentralrs3806471
openSNPrs3806471
23andMers3806471
23andMe allrs3806471
SNP Nexus

SNPshotrs3806471
SNPdbers3806471
MSV3drs3806471
GWAS Ctlgrs3806471
GMAF0.4697
Max Magnitude0
? (A;A) (A;C) (C;C) 28
[PMID 22655090OA-icon.png] ATP-binding cassette transporter G5 and G8 polymorphisms and several environmental factors with serum lipid levels

[PMID 16507104OA-icon.png] A detailed Hapmap of the Sitosterolemia locus spanning 69 kb; differences between Caucasians and African-Americans.


[PMID 19005228OA-icon.png] The effects of ABCG5/G8 polymorphisms on plasma HDL cholesterol concentrations depend on smoking habit in the Boston Puerto Rican Health Study.

ClinVar
Risk rs3806471(C,T;C,T)
Alt rs3806471(C,T;C,T)
Reference rs3806471(A;A)
Significance Non-pathogenic
Disease not specified
Variation info
Gene ABCG5 ABCG8
CLNDBN not specified
Reversed 1
HGVS NC_000002.11:g.44066174T>G
CLNSRC
CLNACC RCV000173521.1,