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rs863224853

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863224853(A;G)
Make rs863224853(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position7736507
GeneCAMTA1
is asnp
is mentioned by
dbSNPrs863224853
ebirs863224853
HLIrs863224853
Exacrs863224853
Varsomers863224853
Maprs863224853
PheGenIrs863224853
hapmaprs863224853
1000 genomesrs863224853
hgdprs863224853
ensemblrs863224853
gopubmedrs863224853
geneviewrs863224853
scholarrs863224853
googlers863224853
pharmgkbrs863224853
gwascentralrs863224853
openSNPrs863224853
23andMers863224853
23andMe allrs863224853
SNP Nexus

SNPshotrs863224853
SNPdbers863224853
MSV3drs863224853
GWAS Ctlgrs863224853
Max Magnitude0
ClinVar
Risk rs863224853(G;G)
Alt rs863224853(G;G)
Reference rs863224853(A;A)
Significance Probable-Pathogenic
Disease Cerebellar ataxia
Variation info
Gene CAMTA1
CLNDBN Cerebellar ataxia, nonprogressive, with mental retardation
Reversed 0
HGVS NC_000001.10:g.7796567A>G
CLNSRC
CLNACC RCV000200068.1,