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rs387906996

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs387906996(A;A)
Make rs387906996(A;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position125997230
GeneCDON
is asnp
is mentioned by
dbSNPrs387906996
ebirs387906996
HLIrs387906996
Exacrs387906996
Varsomers387906996
Maprs387906996
PheGenIrs387906996
hapmaprs387906996
1000 genomesrs387906996
hgdprs387906996
ensemblrs387906996
gopubmedrs387906996
geneviewrs387906996
scholarrs387906996
googlers387906996
pharmgkbrs387906996
gwascentralrs387906996
openSNPrs387906996
23andMers387906996
23andMe allrs387906996
SNP Nexus

SNPshotrs387906996
SNPdbers387906996
MSV3drs387906996
GWAS Ctlgrs387906996
Max Magnitude0
ClinVar
Risk rs387906996(A;A)
Alt rs387906996(A;A)
Reference rs387906996(T;T)
Significance Pathogenic
Disease Holoprosencephaly 11
Variation info
Gene CDON
CLNDBN Holoprosencephaly 11
Reversed 1
HGVS NC_000011.9:g.125867125A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000023727.2,