rs1057519797

Orientation

minus

Stabilized

minus

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

Make rs1057519797(A;A)

Make rs1057519797(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

10

Position

121496705

Gene

FGFR2

is a	snp
is	mentioned by
dbSNP	rs1057519797
dbSNP (classic)	rs1057519797
ClinGen	rs1057519797
ebi	rs1057519797
HLI	rs1057519797
Exac	rs1057519797
Gnomad	rs1057519797
Varsome	rs1057519797
LitVar	rs1057519797
Map	rs1057519797
PheGenI	rs1057519797
Biobank	rs1057519797
1000 genomes	rs1057519797
hgdp	rs1057519797
ensembl	rs1057519797
geneview	rs1057519797
scholar	rs1057519797
google	rs1057519797
pharmgkb	rs1057519797
gwascentral	rs1057519797
openSNP	rs1057519797
23andMe	rs1057519797
SNPshot	rs1057519797
SNPdbe	rs1057519797
MSV3d	rs1057519797
GWAS Ctlg	rs1057519797

Max Magnitude

0

ClinVar
Risk	rs1057519797(A;A)
Alt	rs1057519797(A;A)
Reference	Rs1057519797(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.123256219C>T
CLNSRC
CLNACC	RCV000423825.1,