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rs1057519901

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057519901(A;C)
Make rs1057519901(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position121498525
GeneFGFR2
is asnp
is mentioned by
dbSNPrs1057519901
dbSNP (classic)rs1057519901
ClinGenrs1057519901
ebirs1057519901
HLIrs1057519901
Exacrs1057519901
Gnomadrs1057519901
Varsomers1057519901
LitVarrs1057519901
Maprs1057519901
PheGenIrs1057519901
Biobankrs1057519901
1000 genomesrs1057519901
hgdprs1057519901
ensemblrs1057519901
geneviewrs1057519901
scholarrs1057519901
googlers1057519901
pharmgkbrs1057519901
gwascentralrs1057519901
openSNPrs1057519901
23andMers1057519901
23andMe allrs1057519901
SNPshotrs1057519901
SNPdbers1057519901
MSV3drs1057519901
GWAS Ctlgrs1057519901
Max Magnitude0
ClinVar
Risk rs1057519901(C;C)
Alt rs1057519901(C;C)
Reference Rs1057519901(A;A)
Significance Probable-Pathogenic
Disease Adenocarcinoma of lung Malignant neoplasm of body of uterus Nasopharyngeal Neoplasms Endometrial neoplasm Neoplasm of breast
Variation info
Gene FGFR2
CLNDBN Adenocarcinoma of lung Malignant neoplasm of body of uterus Nasopharyngeal Neoplasms Endometrial neoplasm Neoplasm of breast
Reversed 1
HGVS NC_000010.10:g.123258039T>G
CLNSRC
CLNACC RCV000420899.1, RCV000423679.1, RCV000431121.1, RCV000438545.1, RCV000441378.1,