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rs796065346

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796065346(A;A)
Make rs796065346(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position40935046
GeneDLL4
is asnp
is mentioned by
dbSNPrs796065346
ebirs796065346
HLIrs796065346
Exacrs796065346
Varsomers796065346
Maprs796065346
PheGenIrs796065346
hapmaprs796065346
1000 genomesrs796065346
hgdprs796065346
ensemblrs796065346
gopubmedrs796065346
geneviewrs796065346
scholarrs796065346
googlers796065346
pharmgkbrs796065346
gwascentralrs796065346
openSNPrs796065346
23andMers796065346
23andMe allrs796065346
SNP Nexus

SNPshotrs796065346
SNPdbers796065346
MSV3drs796065346
GWAS Ctlgrs796065346
Max Magnitude0
ClinVar
Risk rs796065346(A;A)
Alt rs796065346(A;A)
Reference rs796065346(G;G)
Significance Pathogenic
Disease Adams-Oliver syndrome Adams-Oliver syndrome 6
Variation info
Gene DLL4
CLNDBN Adams-Oliver syndrome Adams-Oliver syndrome 6
Reversed 0
HGVS NC_000015.9:g.41227244G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000190437.1, RCV000195288.3,