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rs1057519795

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057519795(A;G)
Make rs1057519795(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position121488002
GeneFGFR2
is asnp
is mentioned by
dbSNPrs1057519795
dbSNP (old)rs1057519795
ClinGenrs1057519795
ebirs1057519795
HLIrs1057519795
Exacrs1057519795
Gnomadrs1057519795
Varsomers1057519795
Maprs1057519795
PheGenIrs1057519795
Biobankrs1057519795
1000 genomesrs1057519795
hgdprs1057519795
ensemblrs1057519795
gopubmedrs1057519795
geneviewrs1057519795
scholarrs1057519795
googlers1057519795
pharmgkbrs1057519795
gwascentralrs1057519795
openSNPrs1057519795
23andMers1057519795
23andMe allrs1057519795
SNPshotrs1057519795
SNPdbers1057519795
MSV3drs1057519795
GWAS Ctlgrs1057519795
Max Magnitude0
ClinVar
Risk rs1057519795(G;G)
Alt rs1057519795(G;G)
Reference Rs1057519795(A;A)
Significance Probable-Pathogenic
Disease Endometrial Endometrioid Adenocarcinoma
Variation info
Gene FGFR2
CLNDBN Endometrial Endometrioid Adenocarcinoma, Variant with Squamous Differentiation
Reversed 1
HGVS NC_000010.10:g.123247516T>C
CLNSRC
CLNACC RCV000417597.1,