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rs7597774

From SNPedia

Orientationplus
Stabilizedplus
Make rs7597774(A;A)
Make rs7597774(A;C)
Make rs7597774(C;C)
ReferenceGRCh38 38.1/142
Chromosome2
Position70716718
GeneADD2
is asnp
is mentioned by
dbSNPrs7597774
ebirs7597774
HLIrs7597774
Exacrs7597774
Varsomers7597774
Maprs7597774
PheGenIrs7597774
hapmaprs7597774
1000 genomesrs7597774
hgdprs7597774
ensemblrs7597774
gopubmedrs7597774
geneviewrs7597774
scholarrs7597774
googlers7597774
pharmgkbrs7597774
gwascentralrs7597774
openSNPrs7597774
23andMers7597774
23andMe allrs7597774
SNP Nexus

SNPshotrs7597774
SNPdbers7597774
MSV3drs7597774
GWAS Ctlgrs7597774
Max Magnitude
? (A;A) (A;C) (C;C) 28
[PMID 25785112OA-icon.png] Common variant rs7597774 in ADD2 is associated with dilated cardiomyopathy in Chinese Han population