rs540331226
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs540331226(-;T) |
Make rs540331226(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 3 |
Position | 43605720 |
Gene | ANO10 |
is a | snp |
is | mentioned by |
dbSNP | rs540331226 |
dbSNP (classic) | rs540331226 |
ClinGen | rs540331226 |
ebi | rs540331226 |
HLI | rs540331226 |
Exac | rs540331226 |
Gnomad | rs540331226 |
Varsome | rs540331226 |
LitVar | rs540331226 |
Map | rs540331226 |
PheGenI | rs540331226 |
Biobank | rs540331226 |
1000 genomes | rs540331226 |
hgdp | rs540331226 |
ensembl | rs540331226 |
geneview | rs540331226 |
scholar | rs540331226 |
rs540331226 | |
pharmgkb | rs540331226 |
gwascentral | rs540331226 |
openSNP | rs540331226 |
23andMe | rs540331226 |
SNPshot | rs540331226 |
SNPdbe | rs540331226 |
MSV3d | rs540331226 |
GWAS Ctlg | rs540331226 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs540331226(T;T) |
Alt | rs540331226(T;T) |
Reference | Rs540331226(-;-) |
Significance | Pathogenic |
Disease | Spinocerebellar ataxia not provided |
Variation | info |
Gene | ANO10 |
CLNDBN | Spinocerebellar ataxia, autosomal recessive 10 not provided |
Reversed | 0 |
HGVS | NC_000003.11:g.43647213dupT |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000149437.5, RCV000311100.1, |