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rs876657414

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876657414(A;C)
Make rs876657414(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position98217874
GeneVWA3B
is asnp
is mentioned by
dbSNPrs876657414
ebirs876657414
HLIrs876657414
Exacrs876657414
Varsomers876657414
Maprs876657414
PheGenIrs876657414
hapmaprs876657414
1000 genomesrs876657414
hgdprs876657414
ensemblrs876657414
gopubmedrs876657414
geneviewrs876657414
scholarrs876657414
googlers876657414
pharmgkbrs876657414
gwascentralrs876657414
openSNPrs876657414
23andMers876657414
23andMe allrs876657414
SNP Nexus

SNPshotrs876657414
SNPdbers876657414
MSV3drs876657414
GWAS Ctlgrs876657414
Max Magnitude0
ClinVar
Risk rs876657414(C;C)
Alt rs876657414(C;C)
Reference rs876657414(A;A)
Significance Pathogenic
Disease Spinocerebellar ataxia
Variation info
Gene VWA3B
CLNDBN Spinocerebellar ataxia, autosomal recessive 22
Reversed 0
HGVS NC_000002.11:g.98834337A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000211708.1,