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rs373121544

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 rs373121544(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position71439040
GeneDHCR7
is asnp
is mentioned by
dbSNPrs373121544
dbSNP (old)rs373121544
ClinGenrs373121544
ebirs373121544
HLIrs373121544
Exacrs373121544
Varsomers373121544
Maprs373121544
PheGenIrs373121544
Biobankrs373121544
1000 genomesrs373121544
hgdprs373121544
ensemblrs373121544
gopubmedrs373121544
geneviewrs373121544
scholarrs373121544
googlers373121544
pharmgkbrs373121544
gwascentralrs373121544
openSNPrs373121544
23andMers373121544
23andMe allrs373121544
SNP Nexus

SNPshotrs373121544
SNPdbers373121544
MSV3drs373121544
GWAS Ctlgrs373121544
Max Magnitude3