rs7190823
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs7190823(C;C) |
Make rs7190823(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 89799635 |
Gene | FANCA |
is a | snp |
is | mentioned by |
dbSNP | rs7190823 |
dbSNP (classic) | rs7190823 |
ClinGen | rs7190823 |
ebi | rs7190823 |
HLI | rs7190823 |
Exac | rs7190823 |
Gnomad | rs7190823 |
Varsome | rs7190823 |
LitVar | rs7190823 |
Map | rs7190823 |
PheGenI | rs7190823 |
Biobank | rs7190823 |
1000 genomes | rs7190823 |
hgdp | rs7190823 |
ensembl | rs7190823 |
geneview | rs7190823 |
scholar | rs7190823 |
rs7190823 | |
pharmgkb | rs7190823 |
gwascentral | rs7190823 |
openSNP | rs7190823 |
23andMe | rs7190823 |
SNPshot | rs7190823 |
SNPdbe | rs7190823 |
MSV3d | rs7190823 |
GWAS Ctlg | rs7190823 |
GMAF | 0.3425 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 20386703] Association between DNA damage response and repair genes and risk of invasive serous ovarian cancer.
ClinVar | |
---|---|
Risk | rs7190823(C;C) |
Alt | rs7190823(C;C) |
Reference | Rs7190823(T;T) |
Significance | Non-pathogenic |
Disease | not specified Fanconi anemia |
Variation | info |
Gene | FANCA |
CLNDBN | not specified Fanconi anemia |
Reversed | 0 |
HGVS | NC_000016.9:g.89866043T>C |
CLNSRC | UniProtKB (protein) |
CLNACC | RCV000120967.2, RCV000308742.1, |