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rs12206204

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Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs12206204(C;T)
Make rs12206204(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position26116754
GeneLOC100506979
is asnp
is mentioned by
dbSNPrs12206204
ebirs12206204
HLIrs12206204
Exacrs12206204
Varsomers12206204
Maprs12206204
PheGenIrs12206204
hapmaprs12206204
1000 genomesrs12206204
hgdprs12206204
ensemblrs12206204
gopubmedrs12206204
geneviewrs12206204
scholarrs12206204
googlers12206204
pharmgkbrs12206204
gwascentralrs12206204
openSNPrs12206204
23andMers12206204
23andMe allrs12206204
SNP Nexus

SNPshotrs12206204
SNPdbers12206204
MSV3drs12206204
GWAS Ctlgrs12206204
GMAF0.004132
Max Magnitude0
? (C;C) (C;T) (T;T) 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 T
P-val 8E-7
Odds Ratio 0.18 [0.10-0.26] umol/l increase in log(tbil)


GET Evidence
rs12206204
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.0078125
summary