rs775136381
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs775136381(A;A) |
Make rs775136381(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 3 |
Position | 70976982 |
Gene | FOXP1 |
is a | snp |
is | mentioned by |
dbSNP | rs775136381 |
dbSNP (classic) | rs775136381 |
ClinGen | rs775136381 |
ebi | rs775136381 |
HLI | rs775136381 |
Exac | rs775136381 |
Gnomad | rs775136381 |
Varsome | rs775136381 |
LitVar | rs775136381 |
Map | rs775136381 |
PheGenI | rs775136381 |
Biobank | rs775136381 |
1000 genomes | rs775136381 |
hgdp | rs775136381 |
ensembl | rs775136381 |
geneview | rs775136381 |
scholar | rs775136381 |
rs775136381 | |
pharmgkb | rs775136381 |
gwascentral | rs775136381 |
openSNP | rs775136381 |
23andMe | rs775136381 |
SNPshot | rs775136381 |
SNPdbe | rs775136381 |
MSV3d | rs775136381 |
GWAS Ctlg | rs775136381 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs775136381(A;A) rs775136381(C;C) rs775136381(T;T) |
Alt | rs775136381(A;A) rs775136381(C;C) rs775136381(T;T) |
Reference | Rs775136381(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | FOXP1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000003.11:g.71026133G>A |
CLNSRC | |
CLNACC | RCV000439016.1, |