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rs387906827

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs387906827(C;C)
Make rs387906827(C;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position52397821
GeneORC1
is asnp
is mentioned by
dbSNPrs387906827
ebirs387906827
HLIrs387906827
Exacrs387906827
Varsomers387906827
Maprs387906827
PheGenIrs387906827
hapmaprs387906827
1000 genomesrs387906827
hgdprs387906827
ensemblrs387906827
gopubmedrs387906827
geneviewrs387906827
scholarrs387906827
googlers387906827
pharmgkbrs387906827
gwascentralrs387906827
openSNPrs387906827
23andMers387906827
23andMe allrs387906827
SNP Nexus

SNPshotrs387906827
SNPdbers387906827
MSV3drs387906827
GWAS Ctlgrs387906827
Max Magnitude0
ClinVar
Risk rs387906827(C;C)
Alt rs387906827(C;C)
Reference rs387906827(T;T)
Significance Pathogenic
Disease Meier-Gorlin syndrome 1
Variation info
Gene ORC1
CLNDBN Meier-Gorlin syndrome 1
Reversed 1
HGVS NC_000001.10:g.52863493A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000023155.3,