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rs1986655

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs1986655(A;G)
Make rs1986655(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position125072347
is asnp
is mentioned by
dbSNPrs1986655
ebirs1986655
HLIrs1986655
Exacrs1986655
Varsomers1986655
Maprs1986655
PheGenIrs1986655
hapmaprs1986655
1000 genomesrs1986655
hgdprs1986655
ensemblrs1986655
gopubmedrs1986655
geneviewrs1986655
scholarrs1986655
googlers1986655
pharmgkbrs1986655
gwascentralrs1986655
openSNPrs1986655
23andMers1986655
23andMe allrs1986655
SNP Nexus

SNPshotrs1986655
SNPdbers1986655
MSV3drs1986655
GWAS Ctlgrs1986655
GMAF0.1396
Max Magnitude0
? (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 0.000002
Odds Ratio 0.02 [0.00-0.04] umol/l decrease in log(tbil)


GET Evidence
rs1986655
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.119048
summary