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rs184297154

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common/normal
(G;T) 3 Unaffected carrier of a Smith-Lemli-Opitz syndrome mutation
Make rs184297154(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position71437923
GeneDHCR7
is asnp
is mentioned by
dbSNPrs184297154
ClinGenrs184297154
ebirs184297154
HLIrs184297154
Exacrs184297154
Varsomers184297154
Maprs184297154
PheGenIrs184297154
hapmaprs184297154
1000 genomesrs184297154
hgdprs184297154
ensemblrs184297154
gopubmedrs184297154
geneviewrs184297154
scholarrs184297154
googlers184297154
pharmgkbrs184297154
gwascentralrs184297154
openSNPrs184297154
23andMers184297154
23andMe allrs184297154
SNP Nexus

SNPshotrs184297154
SNPdbers184297154
MSV3drs184297154
GWAS Ctlgrs184297154
Max Magnitude3