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rs271674

From SNPedia

Orientationminus
Stabilizedminus
Make rs271674(A;A)
Make rs271674(A;G)
Make rs271674(G;G)
ReferenceGRCh38 38.1/142
Chromosome17
Position49901622
is asnp
is mentioned by
dbSNPrs271674
ebirs271674
HLIrs271674
Exacrs271674
Varsomers271674
Maprs271674
PheGenIrs271674
hapmaprs271674
1000 genomesrs271674
hgdprs271674
ensemblrs271674
gopubmedrs271674
geneviewrs271674
scholarrs271674
googlers271674
pharmgkbrs271674
gwascentralrs271674
openSNPrs271674
23andMers271674
23andMe allrs271674
SNP Nexus

SNPshotrs271674
SNPdbers271674
MSV3drs271674
GWAS Ctlgrs271674
Max Magnitude
? (A;A) (A;G) (G;G) 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 T
P-val 6E-6
Odds Ratio .03 [NR] unit increase