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rs387906917

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906917(A;A)
Make rs387906917(A;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position88807390
GeneCDT1
is asnp
is mentioned by
dbSNPrs387906917
ebirs387906917
HLIrs387906917
Exacrs387906917
Varsomers387906917
Maprs387906917
PheGenIrs387906917
hapmaprs387906917
1000 genomesrs387906917
hgdprs387906917
ensemblrs387906917
gopubmedrs387906917
geneviewrs387906917
scholarrs387906917
googlers387906917
pharmgkbrs387906917
gwascentralrs387906917
openSNPrs387906917
23andMers387906917
23andMe allrs387906917
SNP Nexus

SNPshotrs387906917
SNPdbers387906917
MSV3drs387906917
GWAS Ctlgrs387906917
Max Magnitude0
ClinVar
Risk rs387906917(A;A)
Alt rs387906917(A;A)
Reference rs387906917(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.88873798G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000023455.5,