rs587779909
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs587779909(A;A) |
Make rs587779909(A;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 9 |
Position | 95135345 |
Gene | C9orf3, FANCC |
is a | snp |
is | mentioned by |
dbSNP | rs587779909 |
dbSNP (classic) | rs587779909 |
ClinGen | rs587779909 |
ebi | rs587779909 |
HLI | rs587779909 |
Exac | rs587779909 |
Gnomad | rs587779909 |
Varsome | rs587779909 |
LitVar | rs587779909 |
Map | rs587779909 |
PheGenI | rs587779909 |
Biobank | rs587779909 |
1000 genomes | rs587779909 |
hgdp | rs587779909 |
ensembl | rs587779909 |
geneview | rs587779909 |
scholar | rs587779909 |
rs587779909 | |
pharmgkb | rs587779909 |
gwascentral | rs587779909 |
openSNP | rs587779909 |
23andMe | rs587779909 |
SNPshot | rs587779909 |
SNPdbe | rs587779909 |
MSV3d | rs587779909 |
GWAS Ctlg | rs587779909 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587779909(A;A) |
Alt | rs587779909(A;A) |
Reference | Rs587779909(G;G) |
Significance | Probable-Pathogenic |
Disease | Fanconi anemia Fanconi anemia |
Variation | info |
Gene | FANCC |
CLNDBN | Fanconi anemia Fanconi anemia, complementation group C |
Reversed | 1 |
HGVS | NC_000009.11:g.97897627C>T |
CLNSRC | |
CLNACC | RCV000204814.1, RCV000410480.1, |