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rs766299724

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;G) 3 Unaffected carrier of a Smith-Lemli-Opitz syndrome mutation
Make rs766299724(A;A)
Make rs766299724(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position71441278
GeneDHCR7
is asnp
is mentioned by
dbSNPrs766299724
dbSNP (old)rs766299724
ClinGenrs766299724
ebirs766299724
HLIrs766299724
Exacrs766299724
Varsomers766299724
Maprs766299724
PheGenIrs766299724
Biobankrs766299724
1000 genomesrs766299724
hgdprs766299724
ensemblrs766299724
gopubmedrs766299724
geneviewrs766299724
scholarrs766299724
googlers766299724
pharmgkbrs766299724
gwascentralrs766299724
openSNPrs766299724
23andMers766299724
23andMe allrs766299724
SNP Nexus

SNPshotrs766299724
SNPdbers766299724
MSV3drs766299724
GWAS Ctlgrs766299724
Max Magnitude3