rs1057520027

Orientation

minus

Stabilized

minus

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

Make rs1057520027(A;G)

Make rs1057520027(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

10

Position

121488005

Gene

FGFR2

is a	snp
is	mentioned by
dbSNP	rs1057520027
dbSNP (classic)	rs1057520027
ClinGen	rs1057520027
ebi	rs1057520027
HLI	rs1057520027
Exac	rs1057520027
Gnomad	rs1057520027
Varsome	rs1057520027
LitVar	rs1057520027
Map	rs1057520027
PheGenI	rs1057520027
Biobank	rs1057520027
1000 genomes	rs1057520027
hgdp	rs1057520027
ensembl	rs1057520027
geneview	rs1057520027
scholar	rs1057520027
google	rs1057520027
pharmgkb	rs1057520027
gwascentral	rs1057520027
openSNP	rs1057520027
23andMe	rs1057520027
SNPshot	rs1057520027
SNPdbe	rs1057520027
MSV3d	rs1057520027
GWAS Ctlg	rs1057520027

Max Magnitude

0

ClinVar
Risk	rs1057520027(G;G)
Alt	rs1057520027(G;G)
Reference	Rs1057520027(A;A)
Significance	Probable-Pathogenic
Disease	Endometrial neoplasm
Variation	info
Gene	FGFR2
CLNDBN	Endometrial neoplasm
Reversed	1
HGVS	NC_000010.10:g.123247519T>C
CLNSRC
CLNACC	RCV000439319.1,