rs1057519800

Orientation

minus

Stabilized

minus

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

Make rs1057519800(G;T)

Make rs1057519800(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

10

Position

121498562

Gene

FGFR2

is a	snp
is	mentioned by
dbSNP	rs1057519800
dbSNP (classic)	rs1057519800
ClinGen	rs1057519800
ebi	rs1057519800
HLI	rs1057519800
Exac	rs1057519800
Gnomad	rs1057519800
Varsome	rs1057519800
LitVar	rs1057519800
Map	rs1057519800
PheGenI	rs1057519800
Biobank	rs1057519800
1000 genomes	rs1057519800
hgdp	rs1057519800
ensembl	rs1057519800
geneview	rs1057519800
scholar	rs1057519800
google	rs1057519800
pharmgkb	rs1057519800
gwascentral	rs1057519800
openSNP	rs1057519800
23andMe	rs1057519800
SNPshot	rs1057519800
SNPdbe	rs1057519800
MSV3d	rs1057519800
GWAS Ctlg	rs1057519800

Max Magnitude

0

ClinVar
Risk	rs1057519800(A;A) rs1057519800(C;C) rs1057519800(T;T)
Alt	rs1057519800(A;A) rs1057519800(C;C) rs1057519800(T;T)
Reference	Rs1057519800(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.123258076C>A; NC_000010.10:g.123258076C>G; NC_000010.10:g.123258076C>T
CLNSRC
CLNACC	RCV000424365.1, RCV000435530.1, RCV000417871.1,