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rs6843082

From SNPedia

Orientationplus
Stabilizedplus
Make rs6843082(A;A)
Make rs6843082(A;G)
Make rs6843082(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position110796911
GeneLOC729065
is asnp
is mentioned by
dbSNPrs6843082
ebirs6843082
HLIrs6843082
Exacrs6843082
Varsomers6843082
Maprs6843082
PheGenIrs6843082
hapmaprs6843082
1000 genomesrs6843082
hgdprs6843082
ensemblrs6843082
gopubmedrs6843082
geneviewrs6843082
scholarrs6843082
googlers6843082
pharmgkbrs6843082
gwascentralrs6843082
openSNPrs6843082
23andMers6843082
23andMe allrs6843082
SNP Nexus

SNPshotrs6843082
SNPdbers6843082
MSV3drs6843082
GWAS Ctlgrs6843082
GMAF0.4082
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20173747OA-icon.png]
Trait Atrial fibrillation
Title Common variants in KCNN3 are associated with lone atrial fibrillation
Risk Allele G
P-val 3E-28
Odds Ratio 2.03 [1.79-2.30]


OMIM611494
Desc
Variant
Relatedalso


GET Evidence
rs6843082
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.625
summary



GWAS snp
PMID [PMID 23041239OA-icon.png]
Trait Stroke (ischemic)
Title Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies.
Risk Allele G
P-val 2E-7
Odds Ratio 1.11 [1.06-1.15]


[PMID 25711478] Association of GWAS-Supported Variants rs2200733 and rs6843082 on Chromosome 4q25 with Ischemic Stroke in the Southern Chinese Han Population


[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)