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rs796065345

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796065345(C;G)
Make rs796065345(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position40936352
GeneDLL4
is asnp
is mentioned by
dbSNPrs796065345
ebirs796065345
HLIrs796065345
Exacrs796065345
Varsomers796065345
Maprs796065345
PheGenIrs796065345
hapmaprs796065345
1000 genomesrs796065345
hgdprs796065345
ensemblrs796065345
gopubmedrs796065345
geneviewrs796065345
scholarrs796065345
googlers796065345
pharmgkbrs796065345
gwascentralrs796065345
openSNPrs796065345
23andMers796065345
23andMe allrs796065345
SNP Nexus

SNPshotrs796065345
SNPdbers796065345
MSV3drs796065345
GWAS Ctlgrs796065345
Max Magnitude0
ClinVar
Risk rs796065345(G;G)
Alt rs796065345(G;G)
Reference rs796065345(C;C)
Significance Pathogenic
Disease Adams-Oliver syndrome
Variation info
Gene DLL4
CLNDBN Adams-Oliver syndrome
Reversed 0
HGVS NC_000015.9:g.41228550C>G
CLNSRC
CLNACC RCV000190436.1,