rs1057519799

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs1057519799(G;T)

Make rs1057519799(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

10

Position

121498556

Gene

FGFR2

is a	snp
is	mentioned by
dbSNP	rs1057519799
dbSNP (classic)	rs1057519799
ClinGen	rs1057519799
ebi	rs1057519799
HLI	rs1057519799
Exac	rs1057519799
Gnomad	rs1057519799
Varsome	rs1057519799
LitVar	rs1057519799
Map	rs1057519799
PheGenI	rs1057519799
Biobank	rs1057519799
1000 genomes	rs1057519799
hgdp	rs1057519799
ensembl	rs1057519799
geneview	rs1057519799
scholar	rs1057519799
google	rs1057519799
pharmgkb	rs1057519799
gwascentral	rs1057519799
openSNP	rs1057519799
23andMe	rs1057519799
SNPshot	rs1057519799
SNPdbe	rs1057519799
MSV3d	rs1057519799
GWAS Ctlg	rs1057519799

Max Magnitude

0

ClinVar
Risk	rs1057519799(A;A) rs1057519799(C;C) rs1057519799(T;T)
Alt	rs1057519799(A;A) rs1057519799(C;C) rs1057519799(T;T)
Reference	Rs1057519799(G;G)
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.123258070C>A; NC_000010.10:g.123258070C>G; NC_000010.10:g.123258070C>T
CLNSRC
CLNACC	RCV000425939.1, RCV000436200.1, RCV000442661.1,