rs1057520029

Orientation

minus

Stabilized

minus

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

Make rs1057520029(A;T)

Make rs1057520029(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

10

Position

121488003

Gene

FGFR2

is a	snp
is	mentioned by
dbSNP	rs1057520029
dbSNP (classic)	rs1057520029
ClinGen	rs1057520029
ebi	rs1057520029
HLI	rs1057520029
Exac	rs1057520029
Gnomad	rs1057520029
Varsome	rs1057520029
LitVar	rs1057520029
Map	rs1057520029
PheGenI	rs1057520029
Biobank	rs1057520029
1000 genomes	rs1057520029
hgdp	rs1057520029
ensembl	rs1057520029
geneview	rs1057520029
scholar	rs1057520029
google	rs1057520029
pharmgkb	rs1057520029
gwascentral	rs1057520029
openSNP	rs1057520029
23andMe	rs1057520029
SNPshot	rs1057520029
SNPdbe	rs1057520029
MSV3d	rs1057520029
GWAS Ctlg	rs1057520029

Max Magnitude

0

ClinVar
Risk	rs1057520029(T;T)
Alt	rs1057520029(T;T)
Reference	Rs1057520029(A;A)
Significance	Probable-Pathogenic
Disease	Endometrial neoplasm
Variation	info
Gene	FGFR2
CLNDBN	Endometrial neoplasm
Reversed	1
HGVS	NC_000010.10:g.123247517T>A
CLNSRC
CLNACC	RCV000433692.1,