rs1057519791

Orientation

minus

Stabilized

minus

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

Make rs1057519791(C;G)

Make rs1057519791(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

10

Position

121518810

Gene

FGFR2

is a	snp
is	mentioned by
dbSNP	rs1057519791
dbSNP (classic)	rs1057519791
ClinGen	rs1057519791
ebi	rs1057519791
HLI	rs1057519791
Exac	rs1057519791
Gnomad	rs1057519791
Varsome	rs1057519791
LitVar	rs1057519791
Map	rs1057519791
PheGenI	rs1057519791
Biobank	rs1057519791
1000 genomes	rs1057519791
hgdp	rs1057519791
ensembl	rs1057519791
geneview	rs1057519791
scholar	rs1057519791
google	rs1057519791
pharmgkb	rs1057519791
gwascentral	rs1057519791
openSNP	rs1057519791
23andMe	rs1057519791
SNPshot	rs1057519791
SNPdbe	rs1057519791
MSV3d	rs1057519791
GWAS Ctlg	rs1057519791

Max Magnitude

0

ClinVar
Risk	rs1057519791(G;G)
Alt	rs1057519791(G;G)
Reference	Rs1057519791(C;C)
Significance	Probable-Pathogenic
Disease	Squamous cell carcinoma of lung
Variation	info
Gene	FGFR2
CLNDBN	Squamous cell carcinoma of lung
Reversed	1
HGVS	NC_000010.10:g.123278324G>C
CLNSRC
CLNACC	RCV000437269.1,