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rs863225297

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863225297(C;G)
Make rs863225297(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position15189278
GeneNOTCH3
is asnp
is mentioned by
dbSNPrs863225297
ebirs863225297
HLIrs863225297
Exacrs863225297
Varsomers863225297
Maprs863225297
PheGenIrs863225297
hapmaprs863225297
1000 genomesrs863225297
hgdprs863225297
ensemblrs863225297
gopubmedrs863225297
geneviewrs863225297
scholarrs863225297
googlers863225297
pharmgkbrs863225297
gwascentralrs863225297
openSNPrs863225297
23andMers863225297
23andMe allrs863225297
SNP Nexus

SNPshotrs863225297
SNPdbers863225297
MSV3drs863225297
GWAS Ctlgrs863225297
Max Magnitude0
ClinVar
Risk rs863225297(G;G)
Alt rs863225297(G;G)
Reference rs863225297(C;C)
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.15300089G>C
CLNSRC
CLNACC RCV000201951.1,