rs878854181
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs878854181(A;A) |
Make rs878854181(A;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 15 |
Position | 89263422 |
Gene | FANCI |
is a | snp |
is | mentioned by |
dbSNP | rs878854181 |
dbSNP (classic) | rs878854181 |
ClinGen | rs878854181 |
ebi | rs878854181 |
HLI | rs878854181 |
Exac | rs878854181 |
Gnomad | rs878854181 |
Varsome | rs878854181 |
LitVar | rs878854181 |
Map | rs878854181 |
PheGenI | rs878854181 |
Biobank | rs878854181 |
1000 genomes | rs878854181 |
hgdp | rs878854181 |
ensembl | rs878854181 |
geneview | rs878854181 |
scholar | rs878854181 |
rs878854181 | |
pharmgkb | rs878854181 |
gwascentral | rs878854181 |
openSNP | rs878854181 |
23andMe | rs878854181 |
SNPshot | rs878854181 |
SNPdbe | rs878854181 |
MSV3d | rs878854181 |
GWAS Ctlg | rs878854181 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs878854181(A;A) |
Alt | rs878854181(A;A) |
Reference | Rs878854181(G;G) |
Significance | Pathogenic |
Disease | Fanconi anemia |
Variation | info |
Gene | FANCI |
CLNDBN | Fanconi anemia |
Reversed | 0 |
HGVS | NC_000015.9:g.89806653G>A |
CLNSRC | |
CLNACC | RCV000230835.1, |