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rs869312969

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312969(G;T)
Make rs869312969(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position52373376
GeneORC1
is asnp
is mentioned by
dbSNPrs869312969
ebirs869312969
HLIrs869312969
Exacrs869312969
Varsomers869312969
Maprs869312969
PheGenIrs869312969
hapmaprs869312969
1000 genomesrs869312969
hgdprs869312969
ensemblrs869312969
gopubmedrs869312969
geneviewrs869312969
scholarrs869312969
googlers869312969
pharmgkbrs869312969
gwascentralrs869312969
openSNPrs869312969
23andMers869312969
23andMe allrs869312969
SNP Nexus

SNPshotrs869312969
SNPdbers869312969
MSV3drs869312969
GWAS Ctlgrs869312969
Max Magnitude0
ClinVar
Risk rs869312969(T;T)
Alt rs869312969(T;T)
Reference rs869312969(G;G)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene ORC1
CLNDBN Inborn genetic diseases
Reversed 1
HGVS NC_000001.10:g.52839048C>A
CLNSRC
CLNACC RCV000210696.1,