rs2190503
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2190503(C;C) |
Make rs2190503(C;T) |
Make rs2190503(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 50674920 |
Gene | GRB10 |
is a | snp |
is | mentioned by |
dbSNP | rs2190503 |
dbSNP (classic) | rs2190503 |
ClinGen | rs2190503 |
ebi | rs2190503 |
HLI | rs2190503 |
Exac | rs2190503 |
Gnomad | rs2190503 |
Varsome | rs2190503 |
LitVar | rs2190503 |
Map | rs2190503 |
PheGenI | rs2190503 |
Biobank | rs2190503 |
1000 genomes | rs2190503 |
hgdp | rs2190503 |
ensembl | rs2190503 |
geneview | rs2190503 |
scholar | rs2190503 |
rs2190503 | |
pharmgkb | rs2190503 |
gwascentral | rs2190503 |
openSNP | rs2190503 |
23andMe | rs2190503 |
SNPshot | rs2190503 |
SNPdbe | rs2190503 |
MSV3d | rs2190503 |
GWAS Ctlg | rs2190503 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 24190013] Genome-wide association study of subtype-specific epithelial ovarian cancer risk alleles using pooled DNA