rs141387386
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs141387386(G;T) |
Make rs141387386(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 17 |
Position | 41819452 |
Gene | FKBP10 |
is a | snp |
is | mentioned by |
dbSNP | rs141387386 |
dbSNP (classic) | rs141387386 |
ClinGen | rs141387386 |
ebi | rs141387386 |
HLI | rs141387386 |
Exac | rs141387386 |
Gnomad | rs141387386 |
Varsome | rs141387386 |
LitVar | rs141387386 |
Map | rs141387386 |
PheGenI | rs141387386 |
Biobank | rs141387386 |
1000 genomes | rs141387386 |
hgdp | rs141387386 |
ensembl | rs141387386 |
geneview | rs141387386 |
scholar | rs141387386 |
rs141387386 | |
pharmgkb | rs141387386 |
gwascentral | rs141387386 |
openSNP | rs141387386 |
23andMe | rs141387386 |
SNPshot | rs141387386 |
SNPdbe | rs141387386 |
MSV3d | rs141387386 |
GWAS Ctlg | rs141387386 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs141387386(T;T) |
Alt | rs141387386(T;T) |
Reference | Rs141387386(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | FKBP10 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000017.10:g.39975704G>T |
CLNSRC | |
CLNACC | RCV000171257.1, |