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rs7604827

From SNPedia

Orientationplus
Stabilizedplus
Make rs7604827(C;C)
Make rs7604827(C;T)
Make rs7604827(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position214477166
GeneVWC2L
is asnp
is mentioned by
dbSNPrs7604827
ebirs7604827
HLIrs7604827
Exacrs7604827
Varsomers7604827
Maprs7604827
PheGenIrs7604827
hapmaprs7604827
1000 genomesrs7604827
hgdprs7604827
ensemblrs7604827
gopubmedrs7604827
geneviewrs7604827
scholarrs7604827
googlers7604827
pharmgkbrs7604827
gwascentralrs7604827
openSNPrs7604827
23andMers7604827
23andMe allrs7604827
SNP Nexus

SNPshotrs7604827
SNPdbers7604827
MSV3drs7604827
GWAS Ctlgrs7604827
GMAF0.1488
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23534349OA-icon.png]
Trait PR interval
Title Generalization of Variants Identified by Genome-Wide Association Studies for Electrocardiographic Traits in African Americans.
Risk Allele C
P-val 5E-6
Odds Ratio 6.54 [NR] ms increase