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rs796065347

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796065347(C;C)
Make rs796065347(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position40935045
GeneDLL4
is asnp
is mentioned by
dbSNPrs796065347
ebirs796065347
HLIrs796065347
Exacrs796065347
Varsomers796065347
Maprs796065347
PheGenIrs796065347
hapmaprs796065347
1000 genomesrs796065347
hgdprs796065347
ensemblrs796065347
gopubmedrs796065347
geneviewrs796065347
scholarrs796065347
googlers796065347
pharmgkbrs796065347
gwascentralrs796065347
openSNPrs796065347
23andMers796065347
23andMe allrs796065347
SNP Nexus

SNPshotrs796065347
SNPdbers796065347
MSV3drs796065347
GWAS Ctlgrs796065347
Max Magnitude0
ClinVar
Risk rs796065347(C;C)
Alt rs796065347(C;C)
Reference rs796065347(T;T)
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.41227243T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000190438.1, RCV000195284.3,