Have questions? Visit https://www.reddit.com/r/SNPedia

rs540331226

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs540331226(-;-)
Make rs540331226(-;T)
Make rs540331226(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position43605720
GeneANO10
is asnp
is mentioned by
dbSNPrs540331226
ebirs540331226
HLIrs540331226
Exacrs540331226
Varsomers540331226
Maprs540331226
PheGenIrs540331226
hapmaprs540331226
1000 genomesrs540331226
hgdprs540331226
ensemblrs540331226
gopubmedrs540331226
geneviewrs540331226
scholarrs540331226
googlers540331226
pharmgkbrs540331226
gwascentralrs540331226
openSNPrs540331226
23andMers540331226
23andMe allrs540331226
SNP Nexus

SNPshotrs540331226
SNPdbers540331226
MSV3drs540331226
GWAS Ctlgrs540331226
Max Magnitude0
ClinVar
Risk rs540331226(T;T)
Alt rs540331226(T;T)
Reference rs540331226(;)
Significance Pathogenic
Disease Spinocerebellar ataxia
Variation info
Gene ANO10
CLNDBN Spinocerebellar ataxia, autosomal recessive 10
Reversed 0
HGVS NC_000003.11:g.43647213dupT
CLNSRC OMIM Allelic Variant
CLNACC RCV000149437.5,