rs1057519798

Orientation

minus

Stabilized

minus

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

Make rs1057519798(A;G)

Make rs1057519798(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

10

Position

121498528

Gene

FGFR2

is a	snp
is	mentioned by
dbSNP	rs1057519798
dbSNP (classic)	rs1057519798
ClinGen	rs1057519798
ebi	rs1057519798
HLI	rs1057519798
Exac	rs1057519798
Gnomad	rs1057519798
Varsome	rs1057519798
LitVar	rs1057519798
Map	rs1057519798
PheGenI	rs1057519798
Biobank	rs1057519798
1000 genomes	rs1057519798
hgdp	rs1057519798
ensembl	rs1057519798
geneview	rs1057519798
scholar	rs1057519798
google	rs1057519798
pharmgkb	rs1057519798
gwascentral	rs1057519798
openSNP	rs1057519798
23andMe	rs1057519798
SNPshot	rs1057519798
SNPdbe	rs1057519798
MSV3d	rs1057519798
GWAS Ctlg	rs1057519798

Max Magnitude

0

ClinVar
Risk	rs1057519798(G;G)
Alt	rs1057519798(G;G)
Reference	Rs1057519798(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.123258042T>C
CLNSRC
CLNACC	RCV000442792.1,