rs387907033
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs387907033(A;A) |
Make rs387907033(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 210155872 |
Gene | SYT14 |
is a | snp |
is | mentioned by |
dbSNP | rs387907033 |
dbSNP (classic) | rs387907033 |
ClinGen | rs387907033 |
ebi | rs387907033 |
HLI | rs387907033 |
Exac | rs387907033 |
Gnomad | rs387907033 |
Varsome | rs387907033 |
LitVar | rs387907033 |
Map | rs387907033 |
PheGenI | rs387907033 |
Biobank | rs387907033 |
1000 genomes | rs387907033 |
hgdp | rs387907033 |
ensembl | rs387907033 |
geneview | rs387907033 |
scholar | rs387907033 |
rs387907033 | |
pharmgkb | rs387907033 |
gwascentral | rs387907033 |
openSNP | rs387907033 |
23andMe | rs387907033 |
SNPshot | rs387907033 |
SNPdbe | rs387907033 |
MSV3d | rs387907033 |
GWAS Ctlg | rs387907033 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs387907033(A;A) rs387907033(C;C) |
Alt | rs387907033(A;A) rs387907033(C;C) |
Reference | Rs387907033(G;G) |
Significance | Pathogenic |
Disease | Spinocerebellar ataxia |
Variation | info |
Gene | SYT14 |
CLNDBN | Spinocerebellar ataxia, autosomal recessive 11 |
Reversed | 0 |
HGVS | NC_000001.10:g.210329217G>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000023846.2, |