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rs587776685

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
(T;T) 0 common in clinvar
Make rs587776685(-;-)
Make rs587776685(-;T)
ReferenceGRCh38 38.1/142
Chromosome13
Position101726732
GeneFGF14
is asnp
is mentioned by
dbSNPrs587776685
ebirs587776685
HLIrs587776685
Exacrs587776685
Varsomers587776685
Maprs587776685
PheGenIrs587776685
hapmaprs587776685
1000 genomesrs587776685
hgdprs587776685
ensemblrs587776685
gopubmedrs587776685
geneviewrs587776685
scholarrs587776685
googlers587776685
pharmgkbrs587776685
gwascentralrs587776685
openSNPrs587776685
23andMers587776685
23andMe allrs587776685
SNP Nexus

SNPshotrs587776685
SNPdbers587776685
MSV3drs587776685
GWAS Ctlgrs587776685
Max Magnitude0
ClinVar
Risk rs587776685(TG,G;TG,G)
Alt rs587776685(TG,G;TG,G)
Reference rs587776685(AG;AG)
Significance Pathogenic
Disease Spinocerebellar ataxia 27
Variation info
Gene FGF14
CLNDBN Spinocerebellar ataxia 27
Reversed 1
HGVS NC_000013.10:g.102379082delT
CLNSRC OMIM Allelic Variant
CLNACC RCV000008585.3,