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rs121912195

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;T) 3 Unaffected carrier of a Smith-Lemli-Opitz syndrome mutation
(T;T) 0 common/normal


Make rs121912195(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position71442349
GeneDHCR7
is asnp
is mentioned by
dbSNPrs121912195
dbSNP (old)rs121912195
ClinGenrs121912195
ebirs121912195
HLIrs121912195
Exacrs121912195
Varsomers121912195
Maprs121912195
PheGenIrs121912195
Biobankrs121912195
1000 genomesrs121912195
hgdprs121912195
ensemblrs121912195
gopubmedrs121912195
geneviewrs121912195
scholarrs121912195
googlers121912195
pharmgkbrs121912195
gwascentralrs121912195
openSNPrs121912195
23andMers121912195
23andMe allrs121912195
SNP Nexus

SNPshotrs121912195
SNPdbers121912195
MSV3drs121912195
GWAS Ctlgrs121912195
Max Magnitude3