rs1057520028

Orientation

minus

Stabilized

minus

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

Make rs1057520028(A;G)

Make rs1057520028(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

10

Position

121515283

Gene

FGFR2

is a	snp
is	mentioned by
dbSNP	rs1057520028
dbSNP (classic)	rs1057520028
ClinGen	rs1057520028
ebi	rs1057520028
HLI	rs1057520028
Exac	rs1057520028
Gnomad	rs1057520028
Varsome	rs1057520028
LitVar	rs1057520028
Map	rs1057520028
PheGenI	rs1057520028
Biobank	rs1057520028
1000 genomes	rs1057520028
hgdp	rs1057520028
ensembl	rs1057520028
geneview	rs1057520028
scholar	rs1057520028
google	rs1057520028
pharmgkb	rs1057520028
gwascentral	rs1057520028
openSNP	rs1057520028
23andMe	rs1057520028
SNPshot	rs1057520028
SNPdbe	rs1057520028
MSV3d	rs1057520028
GWAS Ctlg	rs1057520028

Max Magnitude

0

ClinVar
Risk	rs1057520028(G;G)
Alt	rs1057520028(G;G)
Reference	Rs1057520028(A;A)
Significance	Probable-Pathogenic
Disease	Endometrial neoplasm
Variation	info
Gene	FGFR2
CLNDBN	Endometrial neoplasm
Reversed	1
HGVS	NC_000010.10:g.123274797T>C
CLNSRC
CLNACC	RCV000423432.1,