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rs2622604

From SNPedia

Orientationplus
Stabilizedplus
Make rs2622604(C;C)
Make rs2622604(C;T)
Make rs2622604(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position88157772
GeneABCG2
is asnp
is mentioned by
dbSNPrs2622604
ebirs2622604
HLIrs2622604
Exacrs2622604
Varsomers2622604
Maprs2622604
PheGenIrs2622604
hapmaprs2622604
1000 genomesrs2622604
hgdprs2622604
ensemblrs2622604
gopubmedrs2622604
geneviewrs2622604
scholarrs2622604
googlers2622604
pharmgkbrs2622604
gwascentralrs2622604
openSNPrs2622604
23andMers2622604
23andMe allrs2622604
SNP Nexus

SNPshotrs2622604
SNPdbers2622604
MSV3drs2622604
GWAS Ctlgrs2622604
GMAF0.1832
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 19696792] Single nucleotide polymorphism in ABCG2 is associated with irinotecan-induced severe myelosuppression



GET Evidence
rs2622604
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.78125
summary