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rs3771362

From SNPedia

Orientationplus
Stabilizedplus
Make rs3771362(C;C)
Make rs3771362(C;T)
Make rs3771362(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position198098107
GenePLCL1
is asnp
is mentioned by
dbSNPrs3771362
ebirs3771362
HLIrs3771362
Exacrs3771362
Varsomers3771362
Maprs3771362
PheGenIrs3771362
hapmaprs3771362
1000 genomesrs3771362
hgdprs3771362
ensemblrs3771362
gopubmedrs3771362
geneviewrs3771362
scholarrs3771362
googlers3771362
pharmgkbrs3771362
gwascentralrs3771362
openSNPrs3771362
23andMers3771362
23andMe allrs3771362
SNP Nexus

SNPshotrs3771362
SNPdbers3771362
MSV3drs3771362
GWAS Ctlgrs3771362
GMAF0.1905
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs3771362
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.203125
summary