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rs786205212

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786205212(A;G)
Make rs786205212(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome20
Position1980871
GeneLOC727993, PDYN
is asnp
is mentioned by
dbSNPrs786205212
ebirs786205212
HLIrs786205212
Exacrs786205212
Varsomers786205212
Maprs786205212
PheGenIrs786205212
hapmaprs786205212
1000 genomesrs786205212
hgdprs786205212
ensemblrs786205212
gopubmedrs786205212
geneviewrs786205212
scholarrs786205212
googlers786205212
pharmgkbrs786205212
gwascentralrs786205212
openSNPrs786205212
23andMers786205212
23andMe allrs786205212
SNP Nexus

SNPshotrs786205212
SNPdbers786205212
MSV3drs786205212
GWAS Ctlgrs786205212
Max Magnitude0
ClinVar
Risk rs786205212(G;G)
Alt rs786205212(G;G)
Reference rs786205212(A;A)
Significance Probable-Pathogenic
Disease Spinocerebellar ataxia 23
Variation info
Gene PDYN LOC727993
CLNDBN Spinocerebellar ataxia 23
Reversed 1
HGVS NC_000020.10:g.1961517T>C
CLNSRC
CLNACC RCV000170442.2,