rs863224945
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs863224945(C;C) |
Make rs863224945(C;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 10 |
Position | 95637381 |
Gene | ALDH18A1 |
is a | snp |
is | mentioned by |
dbSNP | rs863224945 |
dbSNP (classic) | rs863224945 |
ClinGen | rs863224945 |
ebi | rs863224945 |
HLI | rs863224945 |
Exac | rs863224945 |
Gnomad | rs863224945 |
Varsome | rs863224945 |
LitVar | rs863224945 |
Map | rs863224945 |
PheGenI | rs863224945 |
Biobank | rs863224945 |
1000 genomes | rs863224945 |
hgdp | rs863224945 |
ensembl | rs863224945 |
geneview | rs863224945 |
scholar | rs863224945 |
rs863224945 | |
pharmgkb | rs863224945 |
gwascentral | rs863224945 |
openSNP | rs863224945 |
23andMe | rs863224945 |
SNPshot | rs863224945 |
SNPdbe | rs863224945 |
MSV3d | rs863224945 |
GWAS Ctlg | rs863224945 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs863224945(C;C) |
Alt | rs863224945(C;C) |
Reference | Rs863224945(T;T) |
Significance | Pathogenic |
Disease | Spastic paraplegia 9 |
Variation | info |
Gene | ALDH18A1 |
CLNDBN | Spastic paraplegia 9 |
Reversed | 1 |
HGVS | NC_000010.10:g.97397138A>G |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000200954.2, |