Have questions? Visit https://www.reddit.com/r/SNPedia

rs894177

From SNPedia

Orientationplus
Stabilizedplus
Make rs894177(A;A)
Make rs894177(A;G)
Make rs894177(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position143175569
GenePBX2P1
is asnp
is mentioned by
dbSNPrs894177
ebirs894177
HLIrs894177
Exacrs894177
Varsomers894177
Maprs894177
PheGenIrs894177
hapmaprs894177
1000 genomesrs894177
hgdprs894177
ensemblrs894177
gopubmedrs894177
geneviewrs894177
scholarrs894177
googlers894177
pharmgkbrs894177
gwascentralrs894177
openSNPrs894177
23andMers894177
23andMe allrs894177
SNP Nexus

SNPshotrs894177
SNPdbers894177
MSV3drs894177
GWAS Ctlgrs894177
GMAF0.2452
Max Magnitude
? (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 G
P-val 0.000003
Odds Ratio 0.28 [NR] unit decrease