rs1057519900

Orientation

minus

Stabilized

minus

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

Make rs1057519900(A;A)

Make rs1057519900(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

10

Position

121515259

Gene

FGFR2

is a	snp
is	mentioned by
dbSNP	rs1057519900
dbSNP (classic)	rs1057519900
ClinGen	rs1057519900
ebi	rs1057519900
HLI	rs1057519900
Exac	rs1057519900
Gnomad	rs1057519900
Varsome	rs1057519900
LitVar	rs1057519900
Map	rs1057519900
PheGenI	rs1057519900
Biobank	rs1057519900
1000 genomes	rs1057519900
hgdp	rs1057519900
ensembl	rs1057519900
geneview	rs1057519900
scholar	rs1057519900
google	rs1057519900
pharmgkb	rs1057519900
gwascentral	rs1057519900
openSNP	rs1057519900
23andMe	rs1057519900
SNPshot	rs1057519900
SNPdbe	rs1057519900
MSV3d	rs1057519900
GWAS Ctlg	rs1057519900

Max Magnitude

0

ClinVar
Risk	rs1057519900(A;A)
Alt	rs1057519900(A;A)
Reference	Rs1057519900(G;G)
Significance	Probable-Pathogenic
Disease	Oesophageal carcinoma Malignant neoplasm of body of uterus Adenocarcinoma of stomach
Variation	info
Gene	FGFR2
CLNDBN	Oesophageal carcinoma Malignant neoplasm of body of uterus Adenocarcinoma of stomach
Reversed	1
HGVS	NC_000010.10:g.123274773C>T
CLNSRC
CLNACC	RCV000421261.1, RCV000434751.1, RCV000438442.1,