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rs863224852

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224852(A;A)
Make rs863224852(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position13359680
GeneCACNA1A
is asnp
is mentioned by
dbSNPrs863224852
ebirs863224852
HLIrs863224852
Exacrs863224852
Varsomers863224852
Maprs863224852
PheGenIrs863224852
hapmaprs863224852
1000 genomesrs863224852
hgdprs863224852
ensemblrs863224852
gopubmedrs863224852
geneviewrs863224852
scholarrs863224852
googlers863224852
pharmgkbrs863224852
gwascentralrs863224852
openSNPrs863224852
23andMers863224852
23andMe allrs863224852
SNP Nexus

SNPshotrs863224852
SNPdbers863224852
MSV3drs863224852
GWAS Ctlgrs863224852
Max Magnitude0
ClinVar
Risk rs863224852(A;A)
Alt rs863224852(A;A)
Reference rs863224852(G;G)
Significance Probable-Pathogenic
Disease Episodic ataxia type 2 Spinocerebellar ataxia 6
Variation info
Gene CACNA1A
CLNDBN Episodic ataxia type 2 Spinocerebellar ataxia 6
Reversed 1
HGVS NC_000019.9:g.13470494C>T
CLNSRC
CLNACC RCV000197857.1,