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rs864621964

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs864621964(A;A)
Make rs864621964(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position15197510
GeneNOTCH3
is asnp
is mentioned by
dbSNPrs864621964
ebirs864621964
HLIrs864621964
Exacrs864621964
Varsomers864621964
Maprs864621964
PheGenIrs864621964
hapmaprs864621964
1000 genomesrs864621964
hgdprs864621964
ensemblrs864621964
gopubmedrs864621964
geneviewrs864621964
scholarrs864621964
googlers864621964
pharmgkbrs864621964
gwascentralrs864621964
openSNPrs864621964
23andMers864621964
23andMe allrs864621964
SNP Nexus

SNPshotrs864621964
SNPdbers864621964
MSV3drs864621964
GWAS Ctlgrs864621964
Max Magnitude0
ClinVar
Risk rs864621964(A;A)
Alt rs864621964(A;A)
Reference rs864621964(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.15308321C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000009802.3,