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rs7900929

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs7900929(A;C)
Make rs7900929(C;C)
ReferenceGRCh38 38.1/142
Chromosome10
Position124896430
is asnp
is mentioned by
dbSNPrs7900929
ebirs7900929
HLIrs7900929
Exacrs7900929
Varsomers7900929
Maprs7900929
PheGenIrs7900929
hapmaprs7900929
1000 genomesrs7900929
hgdprs7900929
ensemblrs7900929
gopubmedrs7900929
geneviewrs7900929
scholarrs7900929
googlers7900929
pharmgkbrs7900929
gwascentralrs7900929
openSNPrs7900929
23andMers7900929
23andMe allrs7900929
SNP Nexus

SNPshotrs7900929
SNPdbers7900929
MSV3drs7900929
GWAS Ctlgrs7900929
GMAF0.1745
Max Magnitude0
? (A;A) (A;C) (C;C) 28


GET Evidence
rs7900929
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.171875
summary