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rs7910620

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs7910620(C;G)
Make rs7910620(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position86087202
GeneGRID1
is asnp
is mentioned by
dbSNPrs7910620
ebirs7910620
HLIrs7910620
Exacrs7910620
Varsomers7910620
Maprs7910620
PheGenIrs7910620
hapmaprs7910620
1000 genomesrs7910620
hgdprs7910620
ensemblrs7910620
gopubmedrs7910620
geneviewrs7910620
scholarrs7910620
googlers7910620
pharmgkbrs7910620
gwascentralrs7910620
openSNPrs7910620
23andMers7910620
23andMe allrs7910620
SNP Nexus

SNPshotrs7910620
SNPdbers7910620
MSV3drs7910620
GWAS Ctlgrs7910620
GMAF0.07117
Max Magnitude0
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 19584346OA-icon.png]
Trait Cardiac structure and function
Title Genetic Variants Associated with Cardiac Structure and Function: A Meta-analysis and Replication of Genome-wide Association Data
Risk Allele G
P-val 7E-7
Odds Ratio 0.17 [0.11-0.23] cm increase


GET Evidence
rs7910620
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.117188
summary