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rs863223881

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223881(A;A)
Make rs863223881(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position41526302
GeneACO2, POLR3H
is asnp
is mentioned by
dbSNPrs863223881
ebirs863223881
HLIrs863223881
Exacrs863223881
Varsomers863223881
Maprs863223881
PheGenIrs863223881
hapmaprs863223881
1000 genomesrs863223881
hgdprs863223881
ensemblrs863223881
gopubmedrs863223881
geneviewrs863223881
scholarrs863223881
googlers863223881
pharmgkbrs863223881
gwascentralrs863223881
openSNPrs863223881
23andMers863223881
23andMe allrs863223881
SNP Nexus

SNPshotrs863223881
SNPdbers863223881
MSV3drs863223881
GWAS Ctlgrs863223881
Max Magnitude0
ClinVar
Risk rs863223881(A;A)
Alt rs863223881(A;A)
Reference rs863223881(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ACO2 POLR3H
CLNDBN not provided
Reversed 0
HGVS NC_000022.10:g.41922306G>A
CLNSRC
CLNACC RCV000197903.1,