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rs10501920

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs10501920(C;G)
Make rs10501920(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position99622442
GeneCNTN5
is asnp
is mentioned by
dbSNPrs10501920
ebirs10501920
HLIrs10501920
Exacrs10501920
Varsomers10501920
Maprs10501920
PheGenIrs10501920
hapmaprs10501920
1000 genomesrs10501920
hgdprs10501920
ensemblrs10501920
gopubmedrs10501920
geneviewrs10501920
scholarrs10501920
googlers10501920
pharmgkbrs10501920
gwascentralrs10501920
openSNPrs10501920
23andMers10501920
23andMe allrs10501920
SNP Nexus

SNPshotrs10501920
SNPdbers10501920
MSV3drs10501920
GWAS Ctlgrs10501920
GMAF0.1478
Max Magnitude0
? (C;C) (C;G) (G;G) 28
GWAS
SNP rs10501920
PubMedID [PMID 17903304OA-icon.png]
Condition Atrial fibrillation
Gene CNTN5
Risk Allele
pValue 9.00E-006
OR NA
95% CI



GET Evidence
rs10501920
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.1875
summary