rs1057519854

Orientation

minus

Stabilized

minus

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

Make rs1057519854(A;A)

Make rs1057519854(A;T)

Reference

GRCh38.p7 38.3/150

Chromosome

10

Position

121488063

Gene

FGFR2

is a	snp
is	mentioned by
dbSNP	rs1057519854
dbSNP (classic)	rs1057519854
ClinGen	rs1057519854
ebi	rs1057519854
HLI	rs1057519854
Exac	rs1057519854
Gnomad	rs1057519854
Varsome	rs1057519854
LitVar	rs1057519854
Map	rs1057519854
PheGenI	rs1057519854
Biobank	rs1057519854
1000 genomes	rs1057519854
hgdp	rs1057519854
ensembl	rs1057519854
geneview	rs1057519854
scholar	rs1057519854
google	rs1057519854
pharmgkb	rs1057519854
gwascentral	rs1057519854
openSNP	rs1057519854
23andMe	rs1057519854
SNPshot	rs1057519854
SNPdbe	rs1057519854
MSV3d	rs1057519854
GWAS Ctlg	rs1057519854

Max Magnitude

0

ClinVar
Risk	rs1057519854(A;A)
Alt	rs1057519854(A;A)
Reference	Rs1057519854(T;T)
Significance	Probable-Pathogenic
Disease	Endometrial neoplasm Neoplasm of breast Adenocarcinoma of lung Nasopharyngeal Neoplasms Malignant neoplasm of body of uterus
Variation	info
Gene	FGFR2
CLNDBN	Endometrial neoplasm Neoplasm of breast Adenocarcinoma of lung Nasopharyngeal Neoplasms Malignant neoplasm of body of uterus
Reversed	1
HGVS	NC_000010.10:g.123247577A>T
CLNSRC
CLNACC	RCV000420097.1, RCV000426084.1, RCV000432646.1, RCV000436783.1, RCV000444404.1,