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rs17030434

From SNPedia

Orientationplus
Stabilizedplus
Make rs17030434(C;C)
Make rs17030434(C;T)
Make rs17030434(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position153782444
GeneSFRP2
is asnp
is mentioned by
dbSNPrs17030434
ebirs17030434
HLIrs17030434
Exacrs17030434
Varsomers17030434
Maprs17030434
PheGenIrs17030434
hapmaprs17030434
1000 genomesrs17030434
hgdprs17030434
ensemblrs17030434
gopubmedrs17030434
geneviewrs17030434
scholarrs17030434
googlers17030434
pharmgkbrs17030434
gwascentralrs17030434
openSNPrs17030434
23andMers17030434
23andMe allrs17030434
SNP Nexus

SNPshotrs17030434
SNPdbers17030434
MSV3drs17030434
GWAS Ctlgrs17030434
GMAF0.2057
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19389651OA-icon.png]
Trait Electrocardiographic conduction measures
Title Genome-wide association study of electrocardiographic conduction measures in an isolated founder population: Kosrae
Risk Allele
P-val 0.000005
Odds Ratio NR NR


GET Evidence
rs17030434
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.132812
summary