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rs10074645

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs10074645(C;T)
Make rs10074645(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position145585822
is asnp
is mentioned by
dbSNPrs10074645
ebirs10074645
HLIrs10074645
Exacrs10074645
Varsomers10074645
Maprs10074645
PheGenIrs10074645
hapmaprs10074645
1000 genomesrs10074645
hgdprs10074645
ensemblrs10074645
gopubmedrs10074645
geneviewrs10074645
scholarrs10074645
googlers10074645
pharmgkbrs10074645
gwascentralrs10074645
openSNPrs10074645
23andMers10074645
23andMe allrs10074645
SNP Nexus

SNPshotrs10074645
SNPdbers10074645
MSV3drs10074645
GWAS Ctlgrs10074645
GMAF0.2043
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 22369142OA-icon.png] Fine mapping of a linkage peak with integration of lipid traits identifies novel coronary artery disease genes on chromosome 5