rs876657387
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs876657387(A;A) |
Make rs876657387(A;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 6 |
Position | 85567567 |
Gene | SNX14 |
is a | snp |
is | mentioned by |
dbSNP | rs876657387 |
dbSNP (classic) | rs876657387 |
ClinGen | rs876657387 |
ebi | rs876657387 |
HLI | rs876657387 |
Exac | rs876657387 |
Gnomad | rs876657387 |
Varsome | rs876657387 |
LitVar | rs876657387 |
Map | rs876657387 |
PheGenI | rs876657387 |
Biobank | rs876657387 |
1000 genomes | rs876657387 |
hgdp | rs876657387 |
ensembl | rs876657387 |
geneview | rs876657387 |
scholar | rs876657387 |
rs876657387 | |
pharmgkb | rs876657387 |
gwascentral | rs876657387 |
openSNP | rs876657387 |
23andMe | rs876657387 |
SNPshot | rs876657387 |
SNPdbe | rs876657387 |
MSV3d | rs876657387 |
GWAS Ctlg | rs876657387 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs876657387(A;A) |
Alt | rs876657387(A;A) |
Reference | Rs876657387(T;T) |
Significance | Pathogenic |
Disease | Spinocerebellar ataxia |
Variation | info |
Gene | SNX14 |
CLNDBN | Spinocerebellar ataxia, autosomal recessive 20 |
Reversed | 1 |
HGVS | NC_000006.11:g.86277285A>T |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000170507.3, |