Have questions? Visit https://www.reddit.com/r/SNPedia

rs17739703

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs17739703(C;C)
Make rs17739703(C;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position32943324
GeneCCDC178
is asnp
is mentioned by
dbSNPrs17739703
ebirs17739703
HLIrs17739703
Exacrs17739703
Varsomers17739703
Maprs17739703
PheGenIrs17739703
hapmaprs17739703
1000 genomesrs17739703
hgdprs17739703
ensemblrs17739703
gopubmedrs17739703
geneviewrs17739703
scholarrs17739703
googlers17739703
pharmgkbrs17739703
gwascentralrs17739703
openSNPrs17739703
23andMers17739703
23andMe allrs17739703
SNP Nexus

SNPshotrs17739703
SNPdbers17739703
MSV3drs17739703
GWAS Ctlgrs17739703
GMAF0.03306
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GET Evidence
rs17739703
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.0078125
summary