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rs864621966

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs864621966(G;T)
Make rs864621966(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position15184451
GeneNOTCH3
is asnp
is mentioned by
dbSNPrs864621966
ebirs864621966
HLIrs864621966
Exacrs864621966
Varsomers864621966
Maprs864621966
PheGenIrs864621966
hapmaprs864621966
1000 genomesrs864621966
hgdprs864621966
ensemblrs864621966
gopubmedrs864621966
geneviewrs864621966
scholarrs864621966
googlers864621966
pharmgkbrs864621966
gwascentralrs864621966
openSNPrs864621966
23andMers864621966
23andMe allrs864621966
SNP Nexus

SNPshotrs864621966
SNPdbers864621966
MSV3drs864621966
GWAS Ctlgrs864621966
Max Magnitude0
ClinVar
Risk rs864621966(T;T)
Alt rs864621966(T;T)
Reference rs864621966(G;G)
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.15295262C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000009807.3,