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

rs17042171

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs17042171(A;A)
Make rs17042171(A;C)
ReferenceGRCh38 38.1/141
Chromosome4
Position110787131
is asnp
is mentioned by
dbSNPrs17042171
ebirs17042171
HLIrs17042171
Exacrs17042171
Varsomers17042171
Maprs17042171
PheGenIrs17042171
hapmaprs17042171
1000 genomesrs17042171
hgdprs17042171
ensemblrs17042171
gopubmedrs17042171
geneviewrs17042171
scholarrs17042171
googlers17042171
pharmgkbrs17042171
gwascentralrs17042171
openSNPrs17042171
23andMers17042171
23andMe allrs17042171
SNP Nexus

SNPshotrs17042171
SNPdbers17042171
MSV3drs17042171
GWAS Ctlgrs17042171
GMAF0.2759
Max Magnitude0
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 19597492OA-icon.png]
Trait Atrial fibrillation
Title Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry
Risk Allele A
P-val 4E-63
Odds Ratio 1.65 None
OMIM611494
Desc
Variant
Relatedalso


GET Evidence
rs17042171
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.234375
summary



[PMID 26467376] Association of rs17042171 with chromosome 4q25 with atrial fibrillation in Chinese Han populations


[PMID 26497660] Novel association of polymorphic genetic variants with predictors of outcome of catheter ablation in atrial fibrillation: new directions from a prospective study (DECAF)