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rs1057519854

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519854(A;A)
Make rs1057519854(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position121488063
GeneFGFR2
is asnp
is mentioned by
dbSNPrs1057519854
dbSNP (old)rs1057519854
ClinGenrs1057519854
ebirs1057519854
HLIrs1057519854
Exacrs1057519854
Gnomadrs1057519854
Varsomers1057519854
LitVarrs1057519854
Maprs1057519854
PheGenIrs1057519854
Biobankrs1057519854
1000 genomesrs1057519854
hgdprs1057519854
ensemblrs1057519854
gopubmedrs1057519854
geneviewrs1057519854
scholarrs1057519854
googlers1057519854
pharmgkbrs1057519854
gwascentralrs1057519854
openSNPrs1057519854
23andMers1057519854
23andMe allrs1057519854
SNPshotrs1057519854
SNPdbers1057519854
MSV3drs1057519854
GWAS Ctlgrs1057519854
Max Magnitude0
ClinVar
Risk rs1057519854(A;A)
Alt rs1057519854(A;A)
Reference Rs1057519854(T;T)
Significance Probable-Pathogenic
Disease Endometrial neoplasm Neoplasm of breast Adenocarcinoma of lung Nasopharyngeal Neoplasms Malignant neoplasm of body of uterus
Variation info
Gene FGFR2
CLNDBN Endometrial neoplasm Neoplasm of breast Adenocarcinoma of lung Nasopharyngeal Neoplasms Malignant neoplasm of body of uterus
Reversed 1
HGVS NC_000010.10:g.123247577A>T
CLNSRC
CLNACC RCV000420097.1, RCV000426084.1, RCV000432646.1, RCV000436783.1, RCV000444404.1,