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rs753960624

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 rs753960624(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position71441383
GeneDHCR7
is asnp
is mentioned by
dbSNPrs753960624
ebirs753960624
HLIrs753960624
Exacrs753960624
Varsomers753960624
Maprs753960624
PheGenIrs753960624
hapmaprs753960624
1000 genomesrs753960624
hgdprs753960624
ensemblrs753960624
gopubmedrs753960624
geneviewrs753960624
scholarrs753960624
googlers753960624
pharmgkbrs753960624
gwascentralrs753960624
openSNPrs753960624
23andMers753960624
23andMe allrs753960624
SNP Nexus

SNPshotrs753960624
SNPdbers753960624
MSV3drs753960624
GWAS Ctlgrs753960624
Max Magnitude3