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rs535561852

From SNPedia

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


Make rs535561852(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position71435476
GeneDHCR7
is asnp
is mentioned by
dbSNPrs535561852
ClinGenrs535561852
ebirs535561852
HLIrs535561852
Exacrs535561852
Varsomers535561852
Maprs535561852
PheGenIrs535561852
hapmaprs535561852
1000 genomesrs535561852
hgdprs535561852
ensemblrs535561852
gopubmedrs535561852
geneviewrs535561852
scholarrs535561852
googlers535561852
pharmgkbrs535561852
gwascentralrs535561852
openSNPrs535561852
23andMers535561852
23andMe allrs535561852
SNP Nexus

SNPshotrs535561852
SNPdbers535561852
MSV3drs535561852
GWAS Ctlgrs535561852
Max Magnitude3