rs104894110
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs104894110(C;T) |
Make rs104894110(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 97854108 |
Gene | FOXE1 |
is a | snp |
is | mentioned by |
dbSNP | rs104894110 |
dbSNP (classic) | rs104894110 |
ClinGen | rs104894110 |
ebi | rs104894110 |
HLI | rs104894110 |
Exac | rs104894110 |
Gnomad | rs104894110 |
Varsome | rs104894110 |
LitVar | rs104894110 |
Map | rs104894110 |
PheGenI | rs104894110 |
Biobank | rs104894110 |
1000 genomes | rs104894110 |
hgdp | rs104894110 |
ensembl | rs104894110 |
geneview | rs104894110 |
scholar | rs104894110 |
rs104894110 | |
pharmgkb | rs104894110 |
gwascentral | rs104894110 |
openSNP | rs104894110 |
23andMe | rs104894110 |
SNPshot | rs104894110 |
SNPdbe | rs104894110 |
MSV3d | rs104894110 |
GWAS Ctlg | rs104894110 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs104894110(T;T) |
Alt | rs104894110(T;T) |
Reference | Rs104894110(C;C) |
Significance | Pathogenic |
Disease | Bamforth syndrome |
Variation | info |
Gene | FOXE1 LOC101928337 |
CLNDBN | Bamforth syndrome |
Reversed | 0 |
HGVS | NC_000009.11:g.100616390C>T |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000007402.5, |