rs886041389
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Chromosome | 16 |
Position | 31191429 |
Gene | FUS |
is a | snp |
is | mentioned by |
dbSNP | rs886041389 |
dbSNP (classic) | rs886041389 |
ClinGen | rs886041389 |
ebi | rs886041389 |
HLI | rs886041389 |
Exac | rs886041389 |
Gnomad | rs886041389 |
Varsome | rs886041389 |
LitVar | rs886041389 |
Map | rs886041389 |
PheGenI | rs886041389 |
Biobank | rs886041389 |
1000 genomes | rs886041389 |
hgdp | rs886041389 |
ensembl | rs886041389 |
geneview | rs886041389 |
scholar | rs886041389 |
rs886041389 | |
pharmgkb | rs886041389 |
gwascentral | rs886041389 |
openSNP | rs886041389 |
23andMe | rs886041389 |
SNPshot | rs886041389 |
SNPdbe | rs886041389 |
MSV3d | rs886041389 |
GWAS Ctlg | rs886041389 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs886041389(C;C) |
Alt | rs886041389(C;C) |
Reference | Rs886041389(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | FUS |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000016.9:g.31202750G>C |
CLNSRC | |
CLNACC | RCV000324584.1, |