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rs1003247

From SNPedia

Orientationminus
Stabilizedminus
Make rs1003247(A;A)
Make rs1003247(A;G)
Make rs1003247(G;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position35570552
is asnp
is mentioned by
dbSNPrs1003247
dbSNP (classic)rs1003247
ClinGenrs1003247
ebirs1003247
HLIrs1003247
Exacrs1003247
Gnomadrs1003247
Varsomers1003247
LitVarrs1003247
Maprs1003247
PheGenIrs1003247
Biobankrs1003247
1000 genomesrs1003247
hgdprs1003247
ensemblrs1003247
geneviewrs1003247
scholarrs1003247
googlers1003247
pharmgkbrs1003247
gwascentralrs1003247
openSNPrs1003247
23andMers1003247
SNPshotrs1003247
SNPdbers1003247
MSV3drs1003247
GWAS Ctlgrs1003247
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 24684796OA-icon.png]
Trait Cognitive function
Title Heritability and genetic association analysis of cognition in the Diabetes Heart Study.
Risk Allele C
P-val 6E-6
Odds Ratio 2.28 [1.31-3.26] unit increase