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rs10115383

From SNPedia

Orientationplus
Stabilizedplus
Make rs10115383(A;A)
Make rs10115383(A;G)
Make rs10115383(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position100608250
is asnp
is mentioned by
dbSNPrs10115383
dbSNP (old)rs10115383
ClinGenrs10115383
ebirs10115383
HLIrs10115383
Exacrs10115383
Varsomers10115383
Maprs10115383
PheGenIrs10115383
Biobankrs10115383
1000 genomesrs10115383
hgdprs10115383
ensemblrs10115383
gopubmedrs10115383
geneviewrs10115383
scholarrs10115383
googlers10115383
pharmgkbrs10115383
gwascentralrs10115383
openSNPrs10115383
23andMers10115383
23andMe allrs10115383
SNP Nexus

SNPshotrs10115383
SNPdbers10115383
MSV3drs10115383
GWAS Ctlgrs10115383
GMAF0.3407
Max Magnitude
? (A;A) (A;G) (G;G) 28


GET Evidence
rs10115383
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.671875
summary