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

rs536394774

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 rs536394774(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position71441308
GeneDHCR7
is asnp
is mentioned by
dbSNPrs536394774
dbSNP (old)rs536394774
ClinGenrs536394774
ebirs536394774
HLIrs536394774
Exacrs536394774
Varsomers536394774
Maprs536394774
PheGenIrs536394774
Biobankrs536394774
1000 genomesrs536394774
hgdprs536394774
ensemblrs536394774
gopubmedrs536394774
geneviewrs536394774
scholarrs536394774
googlers536394774
pharmgkbrs536394774
gwascentralrs536394774
openSNPrs536394774
23andMers536394774
23andMe allrs536394774
SNP Nexus

SNPshotrs536394774
SNPdbers536394774
MSV3drs536394774
GWAS Ctlgrs536394774
Max Magnitude3