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rs387906997

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs387906997(A;G)
Make rs387906997(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position125995047
GeneCDON
is asnp
is mentioned by
dbSNPrs387906997
ebirs387906997
HLIrs387906997
Exacrs387906997
Varsomers387906997
Maprs387906997
PheGenIrs387906997
hapmaprs387906997
1000 genomesrs387906997
hgdprs387906997
ensemblrs387906997
gopubmedrs387906997
geneviewrs387906997
scholarrs387906997
googlers387906997
pharmgkbrs387906997
gwascentralrs387906997
openSNPrs387906997
23andMers387906997
23andMe allrs387906997
SNP Nexus

SNPshotrs387906997
SNPdbers387906997
MSV3drs387906997
GWAS Ctlgrs387906997
Max Magnitude0
ClinVar
Risk rs387906997(G;G)
Alt rs387906997(G;G)
Reference rs387906997(A;A)
Significance Pathogenic
Disease Holoprosencephaly 11
Variation info
Gene CDON
CLNDBN Holoprosencephaly 11
Reversed 1
HGVS NC_000011.9:g.125864942T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000023728.2,