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rs6027755

From SNPedia

Orientationplus
Stabilizedplus
Make rs6027755(A;A)
Make rs6027755(A;G)
Make rs6027755(G;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position60693652
is asnp
is mentioned by
dbSNPrs6027755
ebirs6027755
HLIrs6027755
Exacrs6027755
Varsomers6027755
Maprs6027755
PheGenIrs6027755
hapmaprs6027755
1000 genomesrs6027755
hgdprs6027755
ensemblrs6027755
gopubmedrs6027755
geneviewrs6027755
scholarrs6027755
googlers6027755
pharmgkbrs6027755
gwascentralrs6027755
openSNPrs6027755
23andMers6027755
23andMe allrs6027755
SNP Nexus

SNPshotrs6027755
SNPdbers6027755
MSV3drs6027755
GWAS Ctlgrs6027755
GMAF0.3136
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 A
P-val 0.000006
Odds Ratio 1.09 [NR] unit increase