rs1057519901

Orientation

minus

Stabilized

minus

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

Make rs1057519901(A;C)

Make rs1057519901(C;C)

Reference

GRCh38.p7 38.3/150

Chromosome

10

Position

121498525

Gene

FGFR2

is a	snp
is	mentioned by
dbSNP	rs1057519901
dbSNP (classic)	rs1057519901
ClinGen	rs1057519901
ebi	rs1057519901
HLI	rs1057519901
Exac	rs1057519901
Gnomad	rs1057519901
Varsome	rs1057519901
LitVar	rs1057519901
Map	rs1057519901
PheGenI	rs1057519901
Biobank	rs1057519901
1000 genomes	rs1057519901
hgdp	rs1057519901
ensembl	rs1057519901
geneview	rs1057519901
scholar	rs1057519901
google	rs1057519901
pharmgkb	rs1057519901
gwascentral	rs1057519901
openSNP	rs1057519901
23andMe	rs1057519901
SNPshot	rs1057519901
SNPdbe	rs1057519901
MSV3d	rs1057519901
GWAS Ctlg	rs1057519901

Max Magnitude

0

ClinVar
Risk	rs1057519901(C;C)
Alt	rs1057519901(C;C)
Reference	Rs1057519901(A;A)
Significance	Probable-Pathogenic
Disease	Adenocarcinoma of lung Malignant neoplasm of body of uterus Nasopharyngeal Neoplasms Endometrial neoplasm Neoplasm of breast
Variation	info
Gene	FGFR2
CLNDBN	Adenocarcinoma of lung Malignant neoplasm of body of uterus Nasopharyngeal Neoplasms Endometrial neoplasm Neoplasm of breast
Reversed	1
HGVS	NC_000010.10:g.123258039T>G
CLNSRC
CLNACC	RCV000420899.1, RCV000423679.1, RCV000431121.1, RCV000438545.1, RCV000441378.1,