rs786200949
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs786200949(C;T) |
Make rs786200949(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 2 |
Position | 240788208 |
Gene | KIF1A |
is a | snp |
is | mentioned by |
dbSNP | rs786200949 |
dbSNP (classic) | rs786200949 |
ClinGen | rs786200949 |
ebi | rs786200949 |
HLI | rs786200949 |
Exac | rs786200949 |
Gnomad | rs786200949 |
Varsome | rs786200949 |
LitVar | rs786200949 |
Map | rs786200949 |
PheGenI | rs786200949 |
Biobank | rs786200949 |
1000 genomes | rs786200949 |
hgdp | rs786200949 |
ensembl | rs786200949 |
geneview | rs786200949 |
scholar | rs786200949 |
rs786200949 | |
pharmgkb | rs786200949 |
gwascentral | rs786200949 |
openSNP | rs786200949 |
23andMe | rs786200949 |
SNPshot | rs786200949 |
SNPdbe | rs786200949 |
MSV3d | rs786200949 |
GWAS Ctlg | rs786200949 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs786200949(T;T) |
Alt | rs786200949(T;T) |
Reference | Rs786200949(C;C) |
Significance | Pathogenic |
Disease | Hereditary spastic paraplegia |
Variation | info |
Gene | KIF1A |
CLNDBN | Hereditary spastic paraplegia |
Reversed | 1 |
HGVS | NC_000002.11:g.241727625G>A |
CLNSRC | |
CLNACC | RCV000167867.1, |