rs794727216
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs794727216(A;A) |
Make rs794727216(A;G) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 3 |
Position | 70972550 |
Gene | FOXP1 |
is a | snp |
is | mentioned by |
dbSNP | rs794727216 |
dbSNP (classic) | rs794727216 |
ClinGen | rs794727216 |
ebi | rs794727216 |
HLI | rs794727216 |
Exac | rs794727216 |
Gnomad | rs794727216 |
Varsome | rs794727216 |
LitVar | rs794727216 |
Map | rs794727216 |
PheGenI | rs794727216 |
Biobank | rs794727216 |
1000 genomes | rs794727216 |
hgdp | rs794727216 |
ensembl | rs794727216 |
geneview | rs794727216 |
scholar | rs794727216 |
rs794727216 | |
pharmgkb | rs794727216 |
gwascentral | rs794727216 |
openSNP | rs794727216 |
23andMe | rs794727216 |
SNPshot | rs794727216 |
SNPdbe | rs794727216 |
MSV3d | rs794727216 |
GWAS Ctlg | rs794727216 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs794727216(A;A) |
Alt | rs794727216(A;A) |
Reference | Rs794727216(G;G) |
Significance | Pathogenic |
Disease | not specified not provided |
Variation | info |
Gene | FOXP1 |
CLNDBN | not specified not provided |
Reversed | 1 |
HGVS | NC_000003.11:g.71021701C>T |
CLNSRC | |
CLNACC | RCV000175371.1, RCV000358706.1, |