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rs751604696

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 rs751604696(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position71435466
GeneDHCR7
is asnp
is mentioned by
dbSNPrs751604696
dbSNP (classic)rs751604696
ClinGenrs751604696
ebirs751604696
HLIrs751604696
Exacrs751604696
Gnomadrs751604696
Varsomers751604696
LitVarrs751604696
Maprs751604696
PheGenIrs751604696
Biobankrs751604696
1000 genomesrs751604696
hgdprs751604696
ensemblrs751604696
geneviewrs751604696
scholarrs751604696
googlers751604696
pharmgkbrs751604696
gwascentralrs751604696
openSNPrs751604696
23andMers751604696
SNPshotrs751604696
SNPdbers751604696
MSV3drs751604696
GWAS Ctlgrs751604696
Max Magnitude3
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