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rs774694340

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs774694340(-;-)
Make rs774694340(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position85508043
GeneSNX14
is asnp
is mentioned by
dbSNPrs774694340
ebirs774694340
HLIrs774694340
Exacrs774694340
Varsomers774694340
Maprs774694340
PheGenIrs774694340
hapmaprs774694340
1000 genomesrs774694340
hgdprs774694340
ensemblrs774694340
gopubmedrs774694340
geneviewrs774694340
scholarrs774694340
googlers774694340
pharmgkbrs774694340
gwascentralrs774694340
openSNPrs774694340
23andMers774694340
23andMe allrs774694340
SNP Nexus

SNPshotrs774694340
SNPdbers774694340
MSV3drs774694340
GWAS Ctlgrs774694340
Max Magnitude0
ClinVar
Risk rs774694340(;)
Alt rs774694340(;)
Reference rs774694340(A;A)
Significance Pathogenic
Disease Spinocerebellar ataxia
Variation info
Gene SNX14
CLNDBN Spinocerebellar ataxia, autosomal recessive 20
Reversed 0
HGVS NC_000006.11:g.86217761delA
CLNSRC OMIM Allelic Variant
CLNACC RCV000170508.3,