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rs10481625

From SNPedia

Orientationplus
Stabilizedplus
Make rs10481625(C;C)
Make rs10481625(C;T)
Make rs10481625(T;T)
ReferenceGRCh37 37.1/131
Chromosome9
Position8804761
GenePTPRD
is asnp
is mentioned by
dbSNPrs10481625
ebirs10481625
HLIrs10481625
Exacrs10481625
Varsomers10481625
Maprs10481625
PheGenIrs10481625
hapmaprs10481625
1000 genomesrs10481625
hgdprs10481625
ensemblrs10481625
gopubmedrs10481625
geneviewrs10481625
scholarrs10481625
googlers10481625
pharmgkbrs10481625
gwascentralrs10481625
openSNPrs10481625
23andMers10481625
23andMe allrs10481625
SNP Nexus

SNPshotrs10481625
SNPdbers10481625
MSV3drs10481625
GWAS Ctlgrs10481625
GMAF0.2406
Max Magnitude
? (C;C) (C;T) (T;T) 28



GET Evidence
rs10481625
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.793651
summary