rs104893751
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs104893751(A;A) |
Make rs104893751(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 9750423 |
Gene | OGG1 |
is a | snp |
is | mentioned by |
dbSNP | rs104893751 |
dbSNP (classic) | rs104893751 |
ClinGen | rs104893751 |
ebi | rs104893751 |
HLI | rs104893751 |
Exac | rs104893751 |
Gnomad | rs104893751 |
Varsome | rs104893751 |
LitVar | rs104893751 |
Map | rs104893751 |
PheGenI | rs104893751 |
Biobank | rs104893751 |
1000 genomes | rs104893751 |
hgdp | rs104893751 |
ensembl | rs104893751 |
geneview | rs104893751 |
scholar | rs104893751 |
rs104893751 | |
pharmgkb | rs104893751 |
gwascentral | rs104893751 |
openSNP | rs104893751 |
23andMe | rs104893751 |
SNPshot | rs104893751 |
SNPdbe | rs104893751 |
MSV3d | rs104893751 |
GWAS Ctlg | rs104893751 |
GMAF | 0.0004591 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs104893751(A;A) |
Alt | rs104893751(A;A) |
Reference | Rs104893751(G;G) |
Significance | Pathogenic |
Disease | Clear cell carcinoma of kidney |
Variation | info |
Gene | OGG1 |
CLNDBN | Clear cell carcinoma of kidney |
Reversed | 0 |
HGVS | NC_000003.11:g.9792107G>A |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000008040.4, |