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rs1048612

From SNPedia

Orientationminus
Stabilizedminus
Make rs1048612(C;C)
Make rs1048612(C;T)
Make rs1048612(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position83783414
GeneCDH13
is asnp
is mentioned by
dbSNPrs1048612
ebirs1048612
HLIrs1048612
Exacrs1048612
Varsomers1048612
Maprs1048612
PheGenIrs1048612
hapmaprs1048612
1000 genomesrs1048612
hgdprs1048612
ensemblrs1048612
gopubmedrs1048612
geneviewrs1048612
scholarrs1048612
googlers1048612
pharmgkbrs1048612
gwascentralrs1048612
openSNPrs1048612
23andMers1048612
23andMe allrs1048612
SNP Nexus

SNPshotrs1048612
SNPdbers1048612
MSV3drs1048612
GWAS Ctlgrs1048612
GMAF0.1795
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 24142632OA-icon.png] Association between CDH13 Variants and Cardiometabolic and Vascular Phenotypes in a Korean Population