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rs387906918

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906918(A;A)
Make rs387906918(A;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position88804027
GeneCDT1
is asnp
is mentioned by
dbSNPrs387906918
ebirs387906918
HLIrs387906918
Exacrs387906918
Varsomers387906918
Maprs387906918
PheGenIrs387906918
hapmaprs387906918
1000 genomesrs387906918
hgdprs387906918
ensemblrs387906918
gopubmedrs387906918
geneviewrs387906918
scholarrs387906918
googlers387906918
pharmgkbrs387906918
gwascentralrs387906918
openSNPrs387906918
23andMers387906918
23andMe allrs387906918
SNP Nexus

SNPshotrs387906918
SNPdbers387906918
MSV3drs387906918
GWAS Ctlgrs387906918
Max Magnitude0
ClinVar
Risk rs387906918(A;A)
Alt rs387906918(A;A)
Reference rs387906918(G;G)
Significance Pathogenic
Disease Meier-Gorlin syndrome 4
Variation info
Gene CDT1
CLNDBN Meier-Gorlin syndrome 4
Reversed 0
HGVS NC_000016.9:g.88870435G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000023458.3,