rs1057519045

Orientation

minus

Stabilized

minus

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

Make rs1057519045(A;C)

Make rs1057519045(C;C)

Reference

GRCh38.p7 38.3/150

Chromosome

10

Position

121498522

Gene

FGFR2

is a	snp
is	mentioned by
dbSNP	rs1057519045
dbSNP (classic)	rs1057519045
ClinGen	rs1057519045
ebi	rs1057519045
HLI	rs1057519045
Exac	rs1057519045
Gnomad	rs1057519045
Varsome	rs1057519045
LitVar	rs1057519045
Map	rs1057519045
PheGenI	rs1057519045
Biobank	rs1057519045
1000 genomes	rs1057519045
hgdp	rs1057519045
ensembl	rs1057519045
geneview	rs1057519045
scholar	rs1057519045
google	rs1057519045
pharmgkb	rs1057519045
gwascentral	rs1057519045
openSNP	rs1057519045
23andMe	rs1057519045
SNPshot	rs1057519045
SNPdbe	rs1057519045
MSV3d	rs1057519045
GWAS Ctlg	rs1057519045

Max Magnitude

0

ClinVar
Risk	rs1057519045(C;C)
Alt	rs1057519045(C;C)
Reference	Rs1057519045(A;A)
Significance	Probable-Pathogenic
Disease	Crouzon syndrome Neoplasm of breast Nasopharyngeal Neoplasms Adenocarcinoma of lung Endometrial Endometrioid Adenocarcinoma Malignant neoplasm of body of uterus
Variation	info
Gene	FGFR2
CLNDBN	Crouzon syndrome Neoplasm of breast Nasopharyngeal Neoplasms Adenocarcinoma of lung Endometrial Endometrioid Adenocarcinoma, Variant with Squamous Differentiation Malignant neoplasm of body of uterus
Reversed	1
HGVS	NC_000010.10:g.123258036T>G
CLNSRC
CLNACC	RCV000415507.1, RCV000418082.1, RCV000425472.1, RCV000428300.1, RCV000432507.1, RCV000435736.1,