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rs267606915

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267606915(A;A)
Make rs267606915(A;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position15189085
GeneNOTCH3
is asnp
is mentioned by
dbSNPrs267606915
ebirs267606915
HLIrs267606915
Exacrs267606915
Varsomers267606915
Maprs267606915
PheGenIrs267606915
hapmaprs267606915
1000 genomesrs267606915
hgdprs267606915
ensemblrs267606915
gopubmedrs267606915
geneviewrs267606915
scholarrs267606915
googlers267606915
pharmgkbrs267606915
gwascentralrs267606915
openSNPrs267606915
23andMers267606915
23andMe allrs267606915
SNP Nexus

SNPshotrs267606915
SNPdbers267606915
MSV3drs267606915
GWAS Ctlgrs267606915
Max Magnitude0
ClinVar
Risk rs267606915(A;A)
Alt rs267606915(A;A)
Reference rs267606915(T;T)
Significance Pathogenic
Disease Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
Variation info
Gene NOTCH3
CLNDBN Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
Reversed 1
HGVS NC_000019.9:g.15299896A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000009809.3,