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rs387907033

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387907033(A;A)
Make rs387907033(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position210155872
GeneSYT14
is asnp
is mentioned by
dbSNPrs387907033
ebirs387907033
HLIrs387907033
Exacrs387907033
Varsomers387907033
Maprs387907033
PheGenIrs387907033
hapmaprs387907033
1000 genomesrs387907033
hgdprs387907033
ensemblrs387907033
gopubmedrs387907033
geneviewrs387907033
scholarrs387907033
googlers387907033
pharmgkbrs387907033
gwascentralrs387907033
openSNPrs387907033
23andMers387907033
23andMe allrs387907033
SNP Nexus

SNPshotrs387907033
SNPdbers387907033
MSV3drs387907033
GWAS Ctlgrs387907033
Max Magnitude0
ClinVar
Risk rs387907033(A,C;A,C)
Alt rs387907033(A,C;A,C)
Reference rs387907033(G;G)
Significance Pathogenic
Disease Spinocerebellar ataxia
Variation info
Gene SYT14
CLNDBN Spinocerebellar ataxia, autosomal recessive 11
Reversed 0
HGVS NC_000001.10:g.210329217G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000023846.2,