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rs1014137

From SNPedia

Orientationplus
Stabilizedplus
Make rs1014137(C;C)
Make rs1014137(C;T)
Make rs1014137(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position31584132
GeneCCDC129
is asnp
is mentioned by
dbSNPrs1014137
dbSNP (old)rs1014137
ClinGenrs1014137
ebirs1014137
HLIrs1014137
Exacrs1014137
Gnomadrs1014137
Varsomers1014137
Maprs1014137
PheGenIrs1014137
Biobankrs1014137
1000 genomesrs1014137
hgdprs1014137
ensemblrs1014137
gopubmedrs1014137
geneviewrs1014137
scholarrs1014137
googlers1014137
pharmgkbrs1014137
gwascentralrs1014137
openSNPrs1014137
23andMers1014137
23andMe allrs1014137
SNP Nexus

SNPshotrs1014137
SNPdbers1014137
MSV3drs1014137
GWAS Ctlgrs1014137
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 24578207]
Trait White matter hyperintensity volume in cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy
Title Genome-wide genotyping demonstrates a polygenic risk score associated with white matter hyperintensity volume in CADASIL.
Risk Allele C
P-val 8E-6
Odds Ratio .02 [NR] unit increase