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rs869312957

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312957(C;C)
Make rs869312957(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position52396045
GeneORC1
is asnp
is mentioned by
dbSNPrs869312957
ebirs869312957
HLIrs869312957
Exacrs869312957
Varsomers869312957
Maprs869312957
PheGenIrs869312957
hapmaprs869312957
1000 genomesrs869312957
hgdprs869312957
ensemblrs869312957
gopubmedrs869312957
geneviewrs869312957
scholarrs869312957
googlers869312957
pharmgkbrs869312957
gwascentralrs869312957
openSNPrs869312957
23andMers869312957
23andMe allrs869312957
SNP Nexus

SNPshotrs869312957
SNPdbers869312957
MSV3drs869312957
GWAS Ctlgrs869312957
Max Magnitude0
ClinVar
Risk rs869312957(C;C)
Alt rs869312957(C;C)
Reference rs869312957(G;G)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene ORC1
CLNDBN Inborn genetic diseases
Reversed 1
HGVS NC_000001.10:g.52861717C>G
CLNSRC
CLNACC RCV000210711.1,