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rs777248132

From SNPedia

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


Make rs777248132(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position71438982
GeneDHCR7
is asnp
is mentioned by
dbSNPrs777248132
ClinGenrs777248132
ebirs777248132
HLIrs777248132
Exacrs777248132
Varsomers777248132
Maprs777248132
PheGenIrs777248132
hapmaprs777248132
1000 genomesrs777248132
hgdprs777248132
ensemblrs777248132
gopubmedrs777248132
geneviewrs777248132
scholarrs777248132
googlers777248132
pharmgkbrs777248132
gwascentralrs777248132
openSNPrs777248132
23andMers777248132
23andMe allrs777248132
SNP Nexus

SNPshotrs777248132
SNPdbers777248132
MSV3drs777248132
GWAS Ctlgrs777248132
Max Magnitude3