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rs2607737

From SNPedia

Orientationplus
Stabilizedplus
Make rs2607737(C;C)
Make rs2607737(C;T)
Make rs2607737(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position14151668
GeneXPC
is asnp
is mentioned by
dbSNPrs2607737
ebirs2607737
HLIrs2607737
Exacrs2607737
Varsomers2607737
Maprs2607737
PheGenIrs2607737
hapmaprs2607737
1000 genomesrs2607737
hgdprs2607737
ensemblrs2607737
gopubmedrs2607737
geneviewrs2607737
scholarrs2607737
googlers2607737
pharmgkbrs2607737
gwascentralrs2607737
openSNPrs2607737
23andMers2607737
23andMe allrs2607737
SNP Nexus

SNPshotrs2607737
SNPdbers2607737
MSV3drs2607737
GWAS Ctlgrs2607737
GMAF0.4536
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs2607737
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.390625
summary