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rs766495775

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;G) 3 Unaffected carrier of a Smith-Lemli-Opitz syndrome mutation
(G;G) 0 common/normal
(G;T) 3 Unaffected carrier of a Smith-Lemli-Opitz syndrome mutation


Make rs766495775(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position71437914
GeneDHCR7
is asnp
is mentioned by
dbSNPrs766495775
dbSNP (old)rs766495775
ClinGenrs766495775
ebirs766495775
HLIrs766495775
Exacrs766495775
Gnomadrs766495775
Varsomers766495775
Maprs766495775
PheGenIrs766495775
Biobankrs766495775
1000 genomesrs766495775
hgdprs766495775
ensemblrs766495775
gopubmedrs766495775
geneviewrs766495775
scholarrs766495775
googlers766495775
pharmgkbrs766495775
gwascentralrs766495775
openSNPrs766495775
23andMers766495775
23andMe allrs766495775
SNP Nexus

SNPshotrs766495775
SNPdbers766495775
MSV3drs766495775
GWAS Ctlgrs766495775
Max Magnitude3