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rs387906842

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906842(C;G)
Make rs387906842(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position40294388
GeneCDC6
is asnp
is mentioned by
dbSNPrs387906842
ebirs387906842
HLIrs387906842
Exacrs387906842
Varsomers387906842
Maprs387906842
PheGenIrs387906842
hapmaprs387906842
1000 genomesrs387906842
hgdprs387906842
ensemblrs387906842
gopubmedrs387906842
geneviewrs387906842
scholarrs387906842
googlers387906842
pharmgkbrs387906842
gwascentralrs387906842
openSNPrs387906842
23andMers387906842
23andMe allrs387906842
SNP Nexus

SNPshotrs387906842
SNPdbers387906842
MSV3drs387906842
GWAS Ctlgrs387906842
Max Magnitude0
ClinVar
Risk rs387906842(G;G)
Alt rs387906842(G;G)
Reference rs387906842(C;C)
Significance Pathogenic
Disease Meier-Gorlin syndrome 5
Variation info
Gene CDC6
CLNDBN Meier-Gorlin syndrome 5
Reversed 0
HGVS NC_000017.10:g.38450640C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000023201.3,