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rs7968722

From SNPedia

Orientationplus
Stabilizedplus
Make rs7968722(C;C)
Make rs7968722(C;T)
Make rs7968722(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position84852893
is asnp
is mentioned by
dbSNPrs7968722
ebirs7968722
HLIrs7968722
Exacrs7968722
Varsomers7968722
Maprs7968722
PheGenIrs7968722
hapmaprs7968722
1000 genomesrs7968722
hgdprs7968722
ensemblrs7968722
gopubmedrs7968722
geneviewrs7968722
scholarrs7968722
googlers7968722
pharmgkbrs7968722
gwascentralrs7968722
openSNPrs7968722
23andMers7968722
23andMe allrs7968722
SNP Nexus

SNPshotrs7968722
SNPdbers7968722
MSV3drs7968722
GWAS Ctlgrs7968722
GMAF0.2833
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs7968722
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.375
summary