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rs1048612

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1048612(C;C)
Make rs1048612(C;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position83783414
GeneCDH13
is asnp
is mentioned by
dbSNPrs1048612
dbSNP (old)rs1048612
ClinGenrs1048612
ebirs1048612
HLIrs1048612
Exacrs1048612
Gnomadrs1048612
Varsomers1048612
Maprs1048612
PheGenIrs1048612
Biobankrs1048612
1000 genomesrs1048612
hgdprs1048612
ensemblrs1048612
gopubmedrs1048612
geneviewrs1048612
scholarrs1048612
googlers1048612
pharmgkbrs1048612
gwascentralrs1048612
openSNPrs1048612
23andMers1048612
23andMe allrs1048612
SNP Nexus

SNPshotrs1048612
SNPdbers1048612
MSV3drs1048612
GWAS Ctlgrs1048612
GMAF0.1795
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 24142632OA-icon.png] Association between CDH13 Variants and Cardiometabolic and Vascular Phenotypes in a Korean Population


ClinVar
Risk rs1048612(C;C)
Alt rs1048612(C;C)
Reference Rs1048612(T;T)
Significance Non-pathogenic
Disease not specified
Variation info
Gene CDH13
CLNDBN not specified
Reversed 1
HGVS NC_000016.9:g.83817019A>G
CLNSRC
CLNACC RCV000254546.1,