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rs796065349

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796065349(A;A)
Make rs796065349(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position40932396
GeneDLL4
is asnp
is mentioned by
dbSNPrs796065349
ebirs796065349
HLIrs796065349
Exacrs796065349
Varsomers796065349
Maprs796065349
PheGenIrs796065349
hapmaprs796065349
1000 genomesrs796065349
hgdprs796065349
ensemblrs796065349
gopubmedrs796065349
geneviewrs796065349
scholarrs796065349
googlers796065349
pharmgkbrs796065349
gwascentralrs796065349
openSNPrs796065349
23andMers796065349
23andMe allrs796065349
SNP Nexus

SNPshotrs796065349
SNPdbers796065349
MSV3drs796065349
GWAS Ctlgrs796065349
Max Magnitude0
ClinVar
Risk rs796065349(A;A)
Alt rs796065349(A;A)
Reference rs796065349(C;C)
Significance Pathogenic
Disease Adams-Oliver syndrome
Variation info
Gene DLL4
CLNDBN Adams-Oliver syndrome
Reversed 0
HGVS NC_000015.9:g.41224594C>A
CLNSRC
CLNACC RCV000190440.1,