rs121913475

Orientation

minus

Stabilized

minus

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

Make rs121913475(A;G)

Make rs121913475(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

10

Position

121519989

Gene

FGFR2

is a	snp
is	mentioned by
dbSNP	rs121913475
dbSNP (classic)	rs121913475
ClinGen	rs121913475
ebi	rs121913475
HLI	rs121913475
Exac	rs121913475
Gnomad	rs121913475
Varsome	rs121913475
LitVar	rs121913475
Map	rs121913475
PheGenI	rs121913475
Biobank	rs121913475
1000 genomes	rs121913475
hgdp	rs121913475
ensembl	rs121913475
geneview	rs121913475
scholar	rs121913475
google	rs121913475
pharmgkb	rs121913475
gwascentral	rs121913475
openSNP	rs121913475
23andMe	rs121913475
SNPshot	rs121913475
SNPdbe	rs121913475
MSV3d	rs121913475
GWAS Ctlg	rs121913475

Max Magnitude

0

ClinVar
Risk	rs121913475(G;G)
Alt	rs121913475(G;G)
Reference	Rs121913475(A;A)
Significance	Probable-Pathogenic
Disease	Endometrial neoplasm
Variation	info
Gene	FGFR2
CLNDBN	Endometrial neoplasm
Reversed	1
HGVS	NC_000010.10:g.123279503T>C
CLNSRC
CLNACC	RCV000438031.1,