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rs138659167

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs138659167(C;G)
Make rs138659167(G;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position71435840
GeneDHCR7
is asnp
is mentioned by
dbSNPrs138659167
ebirs138659167
HLIrs138659167
Exacrs138659167
Varsomers138659167
Maprs138659167
PheGenIrs138659167
hapmaprs138659167
1000 genomesrs138659167
hgdprs138659167
ensemblrs138659167
gopubmedrs138659167
geneviewrs138659167
scholarrs138659167
googlers138659167
pharmgkbrs138659167
gwascentralrs138659167
openSNPrs138659167
23andMers138659167
23andMe allrs138659167
SNP Nexus

SNPshotrs138659167
SNPdbers138659167
MSV3drs138659167
GWAS Ctlgrs138659167
Max Magnitude0
ClinVar
Risk rs138659167(A,G;A,G)
Alt rs138659167(A,G;A,G)
Reference rs138659167(C;C)
Significance Other
Disease not provided Smith-Lemli-Opitz syndrome
Variation info
Gene DHCR7
CLNDBN not provided Smith-Lemli-Opitz syndrome
Reversed 0
HGVS NC_000011.9:g.71146886C>G
CLNSRC HGMD
CLNACC RCV000079661.4, RCV000180570.2,