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rs387906969

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs387906969(A;C)
Make rs387906969(C;C)
ReferenceGRCh38 38.1/141
Chromosome16
Position46697521
GeneORC6
is asnp
is mentioned by
dbSNPrs387906969
ebirs387906969
HLIrs387906969
Exacrs387906969
Varsomers387906969
Maprs387906969
PheGenIrs387906969
hapmaprs387906969
1000 genomesrs387906969
hgdprs387906969
ensemblrs387906969
gopubmedrs387906969
geneviewrs387906969
scholarrs387906969
googlers387906969
pharmgkbrs387906969
gwascentralrs387906969
openSNPrs387906969
23andMers387906969
23andMe allrs387906969
SNP Nexus

SNPshotrs387906969
SNPdbers387906969
MSV3drs387906969
GWAS Ctlgrs387906969
Max Magnitude0
ClinVar
Risk rs387906969(C;C)
Alt rs387906969(C;C)
Reference rs387906969(A;A)
Significance Pathogenic
Disease Meier-Gorlin syndrome 3
Variation info
Gene ORC6
CLNDBN Meier-Gorlin syndrome 3
Reversed 0
HGVS NC_000016.9:g.46731433A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000023633.3,