rs780825099
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs780825099(G;G) |
Make rs780825099(G;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 16 |
Position | 89765062 |
Gene | FANCA |
is a | snp |
is | mentioned by |
dbSNP | rs780825099 |
dbSNP (classic) | rs780825099 |
ClinGen | rs780825099 |
ebi | rs780825099 |
HLI | rs780825099 |
Exac | rs780825099 |
Gnomad | rs780825099 |
Varsome | rs780825099 |
LitVar | rs780825099 |
Map | rs780825099 |
PheGenI | rs780825099 |
Biobank | rs780825099 |
1000 genomes | rs780825099 |
hgdp | rs780825099 |
ensembl | rs780825099 |
geneview | rs780825099 |
scholar | rs780825099 |
rs780825099 | |
pharmgkb | rs780825099 |
gwascentral | rs780825099 |
openSNP | rs780825099 |
23andMe | rs780825099 |
SNPshot | rs780825099 |
SNPdbe | rs780825099 |
MSV3d | rs780825099 |
GWAS Ctlg | rs780825099 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs780825099(G;G) |
Alt | rs780825099(G;G) |
Reference | Rs780825099(T;T) |
Significance | Probable-Pathogenic |
Disease | Fanconi anemia |
Variation | info |
Gene | FANCA |
CLNDBN | Fanconi anemia |
Reversed | 0 |
HGVS | NC_000016.9:g.89831470T>G |
CLNSRC | UniProtKB (protein) |
CLNACC | RCV000199923.1, |