rs1057519795

Orientation

minus

Stabilized

minus

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

Make rs1057519795(A;G)

Make rs1057519795(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

10

Position

121488002

Gene

FGFR2

is a	snp
is	mentioned by
dbSNP	rs1057519795
dbSNP (classic)	rs1057519795
ClinGen	rs1057519795
ebi	rs1057519795
HLI	rs1057519795
Exac	rs1057519795
Gnomad	rs1057519795
Varsome	rs1057519795
LitVar	rs1057519795
Map	rs1057519795
PheGenI	rs1057519795
Biobank	rs1057519795
1000 genomes	rs1057519795
hgdp	rs1057519795
ensembl	rs1057519795
geneview	rs1057519795
scholar	rs1057519795
google	rs1057519795
pharmgkb	rs1057519795
gwascentral	rs1057519795
openSNP	rs1057519795
23andMe	rs1057519795
SNPshot	rs1057519795
SNPdbe	rs1057519795
MSV3d	rs1057519795
GWAS Ctlg	rs1057519795

Max Magnitude

0

ClinVar
Risk	rs1057519795(G;G)
Alt	rs1057519795(G;G)
Reference	Rs1057519795(A;A)
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.123247516T>C
CLNSRC
CLNACC	RCV000417597.1,