rs748309520
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs748309520(A;A) |
Make rs748309520(A;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 16 |
Position | 89531903 |
Gene | SPG7 |
is a | snp |
is | mentioned by |
dbSNP | rs748309520 |
dbSNP (classic) | rs748309520 |
ClinGen | rs748309520 |
ebi | rs748309520 |
HLI | rs748309520 |
Exac | rs748309520 |
Gnomad | rs748309520 |
Varsome | rs748309520 |
LitVar | rs748309520 |
Map | rs748309520 |
PheGenI | rs748309520 |
Biobank | rs748309520 |
1000 genomes | rs748309520 |
hgdp | rs748309520 |
ensembl | rs748309520 |
geneview | rs748309520 |
scholar | rs748309520 |
rs748309520 | |
pharmgkb | rs748309520 |
gwascentral | rs748309520 |
openSNP | rs748309520 |
23andMe | rs748309520 |
SNPshot | rs748309520 |
SNPdbe | rs748309520 |
MSV3d | rs748309520 |
GWAS Ctlg | rs748309520 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs748309520(A;A) |
Alt | rs748309520(A;A) |
Reference | Rs748309520(G;G) |
Significance | Other |
Disease | Spastic paraplegia 7 |
Variation | info |
Gene | SPG7 |
CLNDBN | Spastic paraplegia 7 |
Reversed | 0 |
HGVS | NC_000016.9:g.89598311G>A |
CLNSRC | |
CLNACC | RCV000206709.2, |