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rs769951

From SNPedia

Orientationminus
Stabilizedminus
Make rs769951(C;C)
Make rs769951(C;G)
Make rs769951(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position199867267
is asnp
is mentioned by
dbSNPrs769951
ebirs769951
HLIrs769951
Exacrs769951
Varsomers769951
Maprs769951
PheGenIrs769951
hapmaprs769951
1000 genomesrs769951
hgdprs769951
ensemblrs769951
gopubmedrs769951
geneviewrs769951
scholarrs769951
googlers769951
pharmgkbrs769951
gwascentralrs769951
openSNPrs769951
23andMers769951
23andMe allrs769951
SNP Nexus

SNPshotrs769951
SNPdbers769951
MSV3drs769951
GWAS Ctlgrs769951
GMAF0.1524
Max Magnitude
? (C;C) (C;G) (G;G) 28


GET Evidence
rs769951
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.148438
summary