rs755793
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in complete genomics |
Make rs755793(C;C) |
Make rs755793(C;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 121551357 |
Gene | FGFR2 |
is a | snp |
is | mentioned by |
dbSNP | rs755793 |
dbSNP (classic) | rs755793 |
ClinGen | rs755793 |
ebi | rs755793 |
HLI | rs755793 |
Exac | rs755793 |
Gnomad | rs755793 |
Varsome | rs755793 |
LitVar | rs755793 |
Map | rs755793 |
PheGenI | rs755793 |
Biobank | rs755793 |
1000 genomes | rs755793 |
hgdp | rs755793 |
ensembl | rs755793 |
geneview | rs755793 |
scholar | rs755793 |
rs755793 | |
pharmgkb | rs755793 |
gwascentral | rs755793 |
openSNP | rs755793 |
23andMe | rs755793 |
SNPshot | rs755793 |
SNPdbe | rs755793 |
MSV3d | rs755793 |
GWAS Ctlg | rs755793 |
GMAF | 0.1203 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 21382839] Relation of FGFR2 Genetic Polymorphisms to the Association Between Oral Contraceptive Use and the Risk of Breast Cancer in Chinese Women
[PMID 11781872] Genomic screening of fibroblast growth-factor receptor 2 reveals a wide spectrum of mutations in patients with syndromic craniosynostosis.
[PMID 24385678] Involvement of fibroblast growth factor receptor genes in benign prostate hyperplasia in a Korean population
ClinVar | |
---|---|
Risk | rs755793(C;C) |
Alt | rs755793(C;C) |
Reference | Rs755793(T;T) |
Significance | Non-pathogenic |
Disease | not specified Crouzon syndrome not provided |
Variation | info |
Gene | FGFR2 |
CLNDBN | not specified Crouzon syndrome not provided |
Reversed | 1 |
HGVS | NC_000010.10:g.123310871A>G |
CLNSRC | UniProtKB (protein) |
CLNACC | RCV000121066.4, RCV000390607.1, RCV000417413.1, |