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rs656843

From SNPedia

Orientationplus
Make rs656843(C;C)
Make rs656843(C;T)
Make rs656843(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position111194050
GeneDENND2D
is asnp
is mentioned by
dbSNPrs656843
ebirs656843
HLIrs656843
Exacrs656843
Varsomers656843
Maprs656843
PheGenIrs656843
hapmaprs656843
1000 genomesrs656843
hgdprs656843
ensemblrs656843
gopubmedrs656843
geneviewrs656843
scholarrs656843
googlers656843
pharmgkbrs656843
gwascentralrs656843
openSNPrs656843
23andMers656843
23andMe allrs656843
SNP Nexus

SNPshotrs656843
SNPdbers656843
MSV3drs656843
GWAS Ctlgrs656843
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 26509668OA-icon.png] Genetic Variants on Chromosome 1p13.3 Are Associated with Non-ST Elevation Myocardial Infarction and the Expression of DRAM2 in the Finnish Population