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rs755933881

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs755933881(A;A)
Make rs755933881(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position226982969
GeneCOQ8A
is asnp
is mentioned by
dbSNPrs755933881
ebirs755933881
HLIrs755933881
Exacrs755933881
Varsomers755933881
Maprs755933881
PheGenIrs755933881
hapmaprs755933881
1000 genomesrs755933881
hgdprs755933881
ensemblrs755933881
gopubmedrs755933881
geneviewrs755933881
scholarrs755933881
googlers755933881
pharmgkbrs755933881
gwascentralrs755933881
openSNPrs755933881
23andMers755933881
23andMe allrs755933881
SNP Nexus

SNPshotrs755933881
SNPdbers755933881
MSV3drs755933881
GWAS Ctlgrs755933881
Max Magnitude0
ClinVar
Risk rs755933881(A;A)
Alt rs755933881(A;A)
Reference rs755933881(G;G)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene ADCK3
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000001.10:g.227170670G>A
CLNSRC
CLNACC RCV000210650.1,