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rs4773330

From SNPedia

Orientationplus
Stabilizedplus
Make rs4773330(A;A)
Make rs4773330(A;G)
Make rs4773330(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position111166485
GeneARHGEF7
is asnp
is mentioned by
dbSNPrs4773330
ebirs4773330
HLIrs4773330
Exacrs4773330
Varsomers4773330
Maprs4773330
PheGenIrs4773330
hapmaprs4773330
1000 genomesrs4773330
hgdprs4773330
ensemblrs4773330
gopubmedrs4773330
geneviewrs4773330
scholarrs4773330
googlers4773330
pharmgkbrs4773330
gwascentralrs4773330
openSNPrs4773330
23andMers4773330
23andMe allrs4773330
SNP Nexus

SNPshotrs4773330
SNPdbers4773330
MSV3drs4773330
GWAS Ctlgrs4773330
GMAF0.1336
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19414484OA-icon.png]
Trait Serum bilirubin levels
Title Genome-wide association meta-analysis for total serum bilirubin levels
Risk Allele A
P-val 0.000008
Odds Ratio 0.04 [0.02-0.06] umol/l decrease in log(tbil)


GET Evidence
rs4773330
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.882812
summary