rs1057519796

Orientation

minus

Stabilized

minus

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

Make rs1057519796(A;A)

Make rs1057519796(A;T)

Reference

GRCh38.p7 38.3/150

Chromosome

10

Position

121496546

Gene

FGFR2

is a	snp
is	mentioned by
dbSNP	rs1057519796
dbSNP (classic)	rs1057519796
ClinGen	rs1057519796
ebi	rs1057519796
HLI	rs1057519796
Exac	rs1057519796
Gnomad	rs1057519796
Varsome	rs1057519796
LitVar	rs1057519796
Map	rs1057519796
PheGenI	rs1057519796
Biobank	rs1057519796
1000 genomes	rs1057519796
hgdp	rs1057519796
ensembl	rs1057519796
geneview	rs1057519796
scholar	rs1057519796
google	rs1057519796
pharmgkb	rs1057519796
gwascentral	rs1057519796
openSNP	rs1057519796
23andMe	rs1057519796
SNPshot	rs1057519796
SNPdbe	rs1057519796
MSV3d	rs1057519796
GWAS Ctlg	rs1057519796

Max Magnitude

0

ClinVar
Risk	rs1057519796(A;A)
Alt	rs1057519796(A;A)
Reference	Rs1057519796(T;T)
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.123256060A>T
CLNSRC
CLNACC	RCV000428728.1,