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rs35964658

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs35964658(A;G)
Make rs35964658(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position141758435
is asnp
is mentioned by
dbSNPrs35964658
ebirs35964658
HLIrs35964658
Exacrs35964658
Varsomers35964658
Maprs35964658
PheGenIrs35964658
hapmaprs35964658
1000 genomesrs35964658
hgdprs35964658
ensemblrs35964658
gopubmedrs35964658
geneviewrs35964658
scholarrs35964658
googlers35964658
pharmgkbrs35964658
gwascentralrs35964658
openSNPrs35964658
23andMers35964658
23andMe allrs35964658
SNP Nexus

SNPshotrs35964658
SNPdbers35964658
MSV3drs35964658
GWAS Ctlgrs35964658
GMAF0.1942
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GET Evidence
rs35964658
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.148438
summary