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rs1305088

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs1305088(A;A)
Make rs1305088(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position28704313
GeneSLC46A3
is asnp
is mentioned by
dbSNPrs1305088
dbSNP (classic)rs1305088
ClinGenrs1305088
ebirs1305088
HLIrs1305088
Exacrs1305088
Gnomadrs1305088
Varsomers1305088
LitVarrs1305088
Maprs1305088
PheGenIrs1305088
Biobankrs1305088
1000 genomesrs1305088
hgdprs1305088
ensemblrs1305088
geneviewrs1305088
scholarrs1305088
googlers1305088
pharmgkbrs1305088
gwascentralrs1305088
openSNPrs1305088
23andMers1305088
SNPshotrs1305088
SNPdbers1305088
MSV3drs1305088
GWAS Ctlgrs1305088
GMAF0.202
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 20708005OA-icon.png]
Trait
Title Genome-Wide Association Study Identifies Variants Associated with Histologic Features of Nonalcoholic Fatty Liver Disease
Risk Allele A
P-val 0.000009
Odds Ratio 0.58 [NR] unit increase