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rs41309766

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41309766(-;-)
Make rs41309766(-;C)
ReferenceGRCh38 38.1/142
Chromosome9
Position136505384
GeneNOTCH1
is asnp
is mentioned by
dbSNPrs41309766
ebirs41309766
HLIrs41309766
Exacrs41309766
Varsomers41309766
Maprs41309766
PheGenIrs41309766
hapmaprs41309766
1000 genomesrs41309766
hgdprs41309766
ensemblrs41309766
gopubmedrs41309766
geneviewrs41309766
scholarrs41309766
googlers41309766
pharmgkbrs41309766
gwascentralrs41309766
openSNPrs41309766
23andMers41309766
23andMe allrs41309766
SNP Nexus

SNPshotrs41309766
SNPdbers41309766
MSV3drs41309766
GWAS Ctlgrs41309766
Max Magnitude0
ClinVar
Risk rs41309766(;)
Alt rs41309766(;)
Reference rs41309766(C;C)
Significance Pathogenic
Disease Aortic valve disorder
Variation info
Gene NOTCH1
CLNDBN Aortic valve disorder
Reversed 1
HGVS NC_000009.11:g.139399836delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000013295.24,