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rs369673018

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs369673018(G;G)
Make rs369673018(G;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position125984049
GeneCDON
is asnp
is mentioned by
dbSNPrs369673018
ebirs369673018
HLIrs369673018
Exacrs369673018
Varsomers369673018
Maprs369673018
PheGenIrs369673018
hapmaprs369673018
1000 genomesrs369673018
hgdprs369673018
ensemblrs369673018
gopubmedrs369673018
geneviewrs369673018
scholarrs369673018
googlers369673018
pharmgkbrs369673018
gwascentralrs369673018
openSNPrs369673018
23andMers369673018
23andMe allrs369673018
SNP Nexus

SNPshotrs369673018
SNPdbers369673018
MSV3drs369673018
GWAS Ctlgrs369673018
Max Magnitude0
ClinVar
Risk rs369673018(G;G)
Alt rs369673018(G;G)
Reference rs369673018(T;T)
Significance Pathogenic
Disease Holoprosencephaly 11
Variation info
Gene CDON
CLNDBN Holoprosencephaly 11
Reversed 0
HGVS NC_000011.9:g.125853944T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000023729.3,