Have questions? Visit https://www.reddit.com/r/SNPedia

rs61750844

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs61750844(C;T)
Make rs61750844(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position40936659
GeneDLL4
is asnp
is mentioned by
dbSNPrs61750844
ebirs61750844
HLIrs61750844
Exacrs61750844
Varsomers61750844
Maprs61750844
PheGenIrs61750844
hapmaprs61750844
1000 genomesrs61750844
hgdprs61750844
ensemblrs61750844
gopubmedrs61750844
geneviewrs61750844
scholarrs61750844
googlers61750844
pharmgkbrs61750844
gwascentralrs61750844
openSNPrs61750844
23andMers61750844
23andMe allrs61750844
SNP Nexus

SNPshotrs61750844
SNPdbers61750844
MSV3drs61750844
GWAS Ctlgrs61750844
Max Magnitude0
ClinVar
Risk rs61750844(T;T)
Alt rs61750844(T;T)
Reference rs61750844(C;C)
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.41228857C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000190435.1, RCV000195290.3,