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rs17132261

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs17132261(C;T)
Make rs17132261(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position110672513
GeneTMEM232
is asnp
is mentioned by
dbSNPrs17132261
ebirs17132261
HLIrs17132261
Exacrs17132261
Varsomers17132261
Maprs17132261
PheGenIrs17132261
hapmaprs17132261
1000 genomesrs17132261
hgdprs17132261
ensemblrs17132261
gopubmedrs17132261
geneviewrs17132261
scholarrs17132261
googlers17132261
pharmgkbrs17132261
gwascentralrs17132261
openSNPrs17132261
23andMers17132261
23andMe allrs17132261
SNP Nexus

SNPshotrs17132261
SNPdbers17132261
MSV3drs17132261
GWAS Ctlgrs17132261
GMAF0.1102
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19584346OA-icon.png]
Trait Cardiac structure and function
Title Genetic Variants Associated with Cardiac Structure and Function: A Meta-analysis and Replication of Genome-wide Association Data
Risk Allele T
P-val 9E-7
Odds Ratio 0.06 [0.04-0.08] cm increase


GET Evidence
rs17132261
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.104839
summary