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rs773656789

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs773656789(-;-)
Make rs773656789(-;G)
Make rs773656789(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position15160935
GeneNOTCH3
is asnp
is mentioned by
dbSNPrs773656789
ebirs773656789
HLIrs773656789
Exacrs773656789
Varsomers773656789
Maprs773656789
PheGenIrs773656789
hapmaprs773656789
1000 genomesrs773656789
hgdprs773656789
ensemblrs773656789
gopubmedrs773656789
geneviewrs773656789
scholarrs773656789
googlers773656789
pharmgkbrs773656789
gwascentralrs773656789
openSNPrs773656789
23andMers773656789
23andMe allrs773656789
SNP Nexus

SNPshotrs773656789
SNPdbers773656789
MSV3drs773656789
GWAS Ctlgrs773656789
Max Magnitude0
ClinVar
Risk rs773656789(G;G)
Alt rs773656789(G;G)
Reference rs773656789(;)
Significance Pathogenic
Disease Lehman syndrome
Variation info
Gene NOTCH3
CLNDBN Lehman syndrome
Reversed 0
HGVS NC_000019.9:g.15271747dupG
CLNSRC OMIM Allelic Variant
CLNACC RCV000210463.2,