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rs368269558

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common/normal
(C;T) 3 Unaffected carrier of a Smith-Lemli-Opitz syndrome mutation
Make rs368269558(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position71441330
GeneDHCR7
is asnp
is mentioned by
dbSNPrs368269558
ClinGenrs368269558
ebirs368269558
HLIrs368269558
Exacrs368269558
Varsomers368269558
Maprs368269558
PheGenIrs368269558
hapmaprs368269558
1000 genomesrs368269558
hgdprs368269558
ensemblrs368269558
gopubmedrs368269558
geneviewrs368269558
scholarrs368269558
googlers368269558
pharmgkbrs368269558
gwascentralrs368269558
openSNPrs368269558
23andMers368269558
23andMe allrs368269558
SNP Nexus

SNPshotrs368269558
SNPdbers368269558
MSV3drs368269558
GWAS Ctlgrs368269558
Max Magnitude3