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rs387906828

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906828(A;A)
Make rs387906828(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position52375574
GeneORC1
is asnp
is mentioned by
dbSNPrs387906828
ebirs387906828
HLIrs387906828
Exacrs387906828
Varsomers387906828
Maprs387906828
PheGenIrs387906828
hapmaprs387906828
1000 genomesrs387906828
hgdprs387906828
ensemblrs387906828
gopubmedrs387906828
geneviewrs387906828
scholarrs387906828
googlers387906828
pharmgkbrs387906828
gwascentralrs387906828
openSNPrs387906828
23andMers387906828
23andMe allrs387906828
SNP Nexus

SNPshotrs387906828
SNPdbers387906828
MSV3drs387906828
GWAS Ctlgrs387906828
Max Magnitude0
ClinVar
Risk rs387906828(A;A)
Alt rs387906828(A;A)
Reference rs387906828(G;G)
Significance Pathogenic
Disease Meier-Gorlin syndrome 1
Variation info
Gene ORC1
CLNDBN Meier-Gorlin syndrome 1
Reversed 1
HGVS NC_000001.10:g.52841246C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000023157.4,