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rs17031671

From SNPedia

Orientationplus
Stabilizedplus
Make rs17031671(C;C)
Make rs17031671(C;T)
Make rs17031671(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position154468095
GeneDCHS2
is asnp
is mentioned by
dbSNPrs17031671
ebirs17031671
HLIrs17031671
Exacrs17031671
Varsomers17031671
Maprs17031671
PheGenIrs17031671
hapmaprs17031671
1000 genomesrs17031671
hgdprs17031671
ensemblrs17031671
gopubmedrs17031671
geneviewrs17031671
scholarrs17031671
googlers17031671
pharmgkbrs17031671
gwascentralrs17031671
openSNPrs17031671
23andMers17031671
23andMe allrs17031671
SNP Nexus

SNPshotrs17031671
SNPdbers17031671
MSV3drs17031671
GWAS Ctlgrs17031671
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20639394]
Trait Bilirubin levels
Title Genome-wide association of serum bilirubin levels in Korean population.
Risk Allele
P-val 6E-11
Odds Ratio .12 [NR] bilirubin level decrease