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rs7082195

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs7082195(C;T)
Make rs7082195(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position110667691
GeneLOC102724471, RBM20
is asnp
is mentioned by
dbSNPrs7082195
ebirs7082195
HLIrs7082195
Exacrs7082195
Varsomers7082195
Maprs7082195
PheGenIrs7082195
hapmaprs7082195
1000 genomesrs7082195
hgdprs7082195
ensemblrs7082195
gopubmedrs7082195
geneviewrs7082195
scholarrs7082195
googlers7082195
pharmgkbrs7082195
gwascentralrs7082195
openSNPrs7082195
23andMers7082195
23andMe allrs7082195
SNP Nexus

SNPshotrs7082195
SNPdbers7082195
MSV3drs7082195
GWAS Ctlgrs7082195
GMAF0.1331
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GET Evidence
rs7082195
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.132812
summary