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rs387906847

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs387906847(A;G)
Make rs387906847(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position147952440
GeneORC4
is asnp
is mentioned by
dbSNPrs387906847
ebirs387906847
HLIrs387906847
Exacrs387906847
Varsomers387906847
Maprs387906847
PheGenIrs387906847
hapmaprs387906847
1000 genomesrs387906847
hgdprs387906847
ensemblrs387906847
gopubmedrs387906847
geneviewrs387906847
scholarrs387906847
googlers387906847
pharmgkbrs387906847
gwascentralrs387906847
openSNPrs387906847
23andMers387906847
23andMe allrs387906847
SNP Nexus

SNPshotrs387906847
SNPdbers387906847
MSV3drs387906847
GWAS Ctlgrs387906847
Max Magnitude0
ClinVar
Risk rs387906847(G;G)
Alt rs387906847(G;G)
Reference rs387906847(A;A)
Significance Other
Disease Meier-Gorlin syndrome 2
Variation info
Gene ORC4
CLNDBN Meier-Gorlin syndrome 2
Reversed 1
HGVS NC_000002.11:g.148710009T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000023230.5,