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rs755793

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs755793(C;C)
Make rs755793(C;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position121551357
GeneFGFR2
is asnp
is mentioned by
dbSNPrs755793
ebirs755793
HLIrs755793
Exacrs755793
Varsomers755793
Maprs755793
PheGenIrs755793
hapmaprs755793
1000 genomesrs755793
hgdprs755793
ensemblrs755793
gopubmedrs755793
geneviewrs755793
scholarrs755793
googlers755793
pharmgkbrs755793
gwascentralrs755793
openSNPrs755793
23andMers755793
23andMe allrs755793
SNP Nexus

SNPshotrs755793
SNPdbers755793
MSV3drs755793
GWAS Ctlgrs755793
GMAF0.1203
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 21382839OA-icon.png] Relation of FGFR2 Genetic Polymorphisms to the Association Between Oral Contraceptive Use and the Risk of Breast Cancer in Chinese Women


[PMID 11781872OA-icon.png] Genomic screening of fibroblast growth-factor receptor 2 reveals a wide spectrum of mutations in patients with syndromic craniosynostosis.


GET Evidence
FGFR2-M186T
aa_change Met186Thr
aa_change_short M186T
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.103923
summary



[PMID 24385678OA-icon.png] 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 Untested
Disease not specified
Variation info
Gene FGFR2
CLNDBN not specified
Reversed 1
HGVS NC_000010.10:g.123310871A>G
CLNSRC ClinVar
CLNACC RCV000121066.1,