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rs761458977

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common/normal
(A;G) 3 Unaffected carrier of a Smith-Lemli-Opitz syndrome mutation
Make rs761458977(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position71435452
GeneDHCR7
is asnp
is mentioned by
dbSNPrs761458977
dbSNP (old)rs761458977
ClinGenrs761458977
ebirs761458977
HLIrs761458977
Exacrs761458977
Varsomers761458977
Maprs761458977
PheGenIrs761458977
Biobankrs761458977
1000 genomesrs761458977
hgdprs761458977
ensemblrs761458977
gopubmedrs761458977
geneviewrs761458977
scholarrs761458977
googlers761458977
pharmgkbrs761458977
gwascentralrs761458977
openSNPrs761458977
23andMers761458977
23andMe allrs761458977
SNP Nexus

SNPshotrs761458977
SNPdbers761458977
MSV3drs761458977
GWAS Ctlgrs761458977
Max Magnitude3