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rs7722600

From SNPedia

Orientationplus
Stabilizedplus
Make rs7722600(A;A)
Make rs7722600(A;G)
Make rs7722600(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position137859073
GeneLOC101928005
is asnp
is mentioned by
dbSNPrs7722600
ebirs7722600
HLIrs7722600
Exacrs7722600
Varsomers7722600
Maprs7722600
PheGenIrs7722600
hapmaprs7722600
1000 genomesrs7722600
hgdprs7722600
ensemblrs7722600
gopubmedrs7722600
geneviewrs7722600
scholarrs7722600
googlers7722600
pharmgkbrs7722600
gwascentralrs7722600
openSNPrs7722600
23andMers7722600
23andMe allrs7722600
SNP Nexus

SNPshotrs7722600
SNPdbers7722600
MSV3drs7722600
GWAS Ctlgrs7722600
GMAF0.1345
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23583979OA-icon.png]
Trait Heart rate
Title Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.
Risk Allele A
P-val 3E-7
Odds Ratio NR NR
? (A;A) (A;G) (G;G)