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rs10116682

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs10116682(A;A)
Make rs10116682(A;C)
ReferenceGRCh37 37.1/131
Chromosome9
Position8761778
GenePTPRD
is asnp
is mentioned by
dbSNPrs10116682
ebirs10116682
HLIrs10116682
Exacrs10116682
Varsomers10116682
Maprs10116682
PheGenIrs10116682
hapmaprs10116682
1000 genomesrs10116682
hgdprs10116682
ensemblrs10116682
gopubmedrs10116682
geneviewrs10116682
scholarrs10116682
googlers10116682
pharmgkbrs10116682
gwascentralrs10116682
openSNPrs10116682
23andMers10116682
23andMe allrs10116682
SNP Nexus

SNPshotrs10116682
SNPdbers10116682
MSV3drs10116682
GWAS Ctlgrs10116682
GMAF0.05234
Max Magnitude0
? (A;A) (A;C) (C;C) 28


GET Evidence
rs10116682
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.0703125
summary