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rs17222723

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common on affy axiom data
Make rs17222723(A;A)
Make rs17222723(A;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position99836239
GeneABCC2
is asnp
is mentioned by
dbSNPrs17222723
ebirs17222723
HLIrs17222723
Exacrs17222723
Varsomers17222723
Maprs17222723
PheGenIrs17222723
hapmaprs17222723
1000 genomesrs17222723
hgdprs17222723
ensemblrs17222723
gopubmedrs17222723
geneviewrs17222723
scholarrs17222723
googlers17222723
pharmgkbrs17222723
gwascentralrs17222723
openSNPrs17222723
23andMers17222723
23andMe allrs17222723
SNP Nexus

SNPshotrs17222723
SNPdbers17222723
MSV3drs17222723
GWAS Ctlgrs17222723
GMAF0.0427
Max Magnitude0
? (A;T) (T;T)


[PMID 17997497] Association of the multidrug-resistance-associated protein gene (ABCC2) variants with intrahepatic cholestasis of pregnancy.


[PMID 18176959OA-icon.png] Increased susceptibility for intrahepatic cholestasis of pregnancy and contraceptive-induced cholestasis in carriers of the 1331T>C polymorphism in the bile salt export pump.


[PMID 18395921OA-icon.png] Role of ABCC2 common variants in intrahepatic cholestasis of pregnancy.


[PMID 18926681] Polymorphisms of MRP2 (ABCC2) are associated with susceptibility to nonalcoholic fatty liver disease.


GET Evidence
ABCC2-V1188E
aa_change Val1188Glu
aa_change_short V1188E
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.0620004
summary