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rs587782989

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587782989(A;A)
Make rs587782989(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position91321256
GeneCCDC88C
is asnp
is mentioned by
dbSNPrs587782989
ebirs587782989
HLIrs587782989
Exacrs587782989
Varsomers587782989
Maprs587782989
PheGenIrs587782989
hapmaprs587782989
1000 genomesrs587782989
hgdprs587782989
ensemblrs587782989
gopubmedrs587782989
geneviewrs587782989
scholarrs587782989
googlers587782989
pharmgkbrs587782989
gwascentralrs587782989
openSNPrs587782989
23andMers587782989
23andMe allrs587782989
SNP Nexus

SNPshotrs587782989
SNPdbers587782989
MSV3drs587782989
GWAS Ctlgrs587782989
Max Magnitude0
ClinVar
Risk rs587782989(A;A)
Alt rs587782989(A;A)
Reference rs587782989(G;G)
Significance Pathogenic
Disease Spinocerebellar ataxia 40
Variation info
Gene CCDC88C
CLNDBN Spinocerebellar ataxia 40
Reversed 1
HGVS NC_000014.8:g.91787600C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000143996.3,