rs781542763
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs781542763(A;A) |
Make rs781542763(A;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 9 |
Position | 95171080 |
Gene | FANCC |
is a | snp |
is | mentioned by |
dbSNP | rs781542763 |
dbSNP (classic) | rs781542763 |
ClinGen | rs781542763 |
ebi | rs781542763 |
HLI | rs781542763 |
Exac | rs781542763 |
Gnomad | rs781542763 |
Varsome | rs781542763 |
LitVar | rs781542763 |
Map | rs781542763 |
PheGenI | rs781542763 |
Biobank | rs781542763 |
1000 genomes | rs781542763 |
hgdp | rs781542763 |
ensembl | rs781542763 |
geneview | rs781542763 |
scholar | rs781542763 |
rs781542763 | |
pharmgkb | rs781542763 |
gwascentral | rs781542763 |
openSNP | rs781542763 |
23andMe | rs781542763 |
SNPshot | rs781542763 |
SNPdbe | rs781542763 |
MSV3d | rs781542763 |
GWAS Ctlg | rs781542763 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs781542763(A;A) |
Alt | rs781542763(A;A) |
Reference | Rs781542763(G;G) |
Significance | Probable-Pathogenic |
Disease | Fanconi anemia |
Variation | info |
Gene | FANCC |
CLNDBN | Fanconi anemia, complementation group C |
Reversed | 0 |
HGVS | NC_000009.11:g.97933362G>A |
CLNSRC | |
CLNACC | RCV000169411.1, |