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rs12542166

From SNPedia

Orientationplus
Stabilizedplus
Make rs12542166(A;A)
Make rs12542166(A;C)
Make rs12542166(C;C)
ReferenceGRCh38 38.1/142
Chromosome8
Position121970599
is asnp
is mentioned by
dbSNPrs12542166
ebirs12542166
HLIrs12542166
Exacrs12542166
Varsomers12542166
Maprs12542166
PheGenIrs12542166
hapmaprs12542166
1000 genomesrs12542166
hgdprs12542166
ensemblrs12542166
gopubmedrs12542166
geneviewrs12542166
scholarrs12542166
googlers12542166
pharmgkbrs12542166
gwascentralrs12542166
openSNPrs12542166
23andMers12542166
23andMe allrs12542166
SNP Nexus

SNPshotrs12542166
SNPdbers12542166
MSV3drs12542166
GWAS Ctlgrs12542166
Max Magnitude
? (A;A) (A;C) (C;C) 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 6E-6
Odds Ratio .11 [NR] unit increase