rs758385503
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs758385503(-;-) |
Make rs758385503(-;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 17 |
Position | 17228089 |
Gene | FLCN |
is a | snp |
is | mentioned by |
dbSNP | rs758385503 |
dbSNP (classic) | rs758385503 |
ClinGen | rs758385503 |
ebi | rs758385503 |
HLI | rs758385503 |
Exac | rs758385503 |
Gnomad | rs758385503 |
Varsome | rs758385503 |
LitVar | rs758385503 |
Map | rs758385503 |
PheGenI | rs758385503 |
Biobank | rs758385503 |
1000 genomes | rs758385503 |
hgdp | rs758385503 |
ensembl | rs758385503 |
geneview | rs758385503 |
scholar | rs758385503 |
rs758385503 | |
pharmgkb | rs758385503 |
gwascentral | rs758385503 |
openSNP | rs758385503 |
23andMe | rs758385503 |
SNPshot | rs758385503 |
SNPdbe | rs758385503 |
MSV3d | rs758385503 |
GWAS Ctlg | rs758385503 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs758385503(-;-) |
Alt | rs758385503(-;-) |
Reference | Rs758385503(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | FLCN |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000017.10:g.17131403delG |
CLNSRC | |
CLNACC | RCV000485925.1, |