rs886041355
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Chromosome | 6 |
Position | 1610901 |
Gene | FOXC1 |
is a | snp |
is | mentioned by |
dbSNP | rs886041355 |
dbSNP (classic) | rs886041355 |
ClinGen | rs886041355 |
ebi | rs886041355 |
HLI | rs886041355 |
Exac | rs886041355 |
Gnomad | rs886041355 |
Varsome | rs886041355 |
LitVar | rs886041355 |
Map | rs886041355 |
PheGenI | rs886041355 |
Biobank | rs886041355 |
1000 genomes | rs886041355 |
hgdp | rs886041355 |
ensembl | rs886041355 |
geneview | rs886041355 |
scholar | rs886041355 |
rs886041355 | |
pharmgkb | rs886041355 |
gwascentral | rs886041355 |
openSNP | rs886041355 |
23andMe | rs886041355 |
SNPshot | rs886041355 |
SNPdbe | rs886041355 |
MSV3d | rs886041355 |
GWAS Ctlg | rs886041355 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs886041355(A;A) |
Alt | rs886041355(A;A) |
Reference | Rs886041355(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | FOXC1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000006.11:g.1611136G>A |
CLNSRC | |
CLNACC | RCV000330423.1, |