rs121913476

Orientation

minus

Stabilized

minus

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

Make rs121913476(A;A)

Make rs121913476(A;T)

Reference

GRCh38.p7 38.3/150

Chromosome

10

Position

121498520

Gene

FGFR2

is a	snp
is	mentioned by
dbSNP	rs121913476
dbSNP (classic)	rs121913476
ClinGen	rs121913476
ebi	rs121913476
HLI	rs121913476
Exac	rs121913476
Gnomad	rs121913476
Varsome	rs121913476
LitVar	rs121913476
Map	rs121913476
PheGenI	rs121913476
Biobank	rs121913476
1000 genomes	rs121913476
hgdp	rs121913476
ensembl	rs121913476
geneview	rs121913476
scholar	rs121913476
google	rs121913476
pharmgkb	rs121913476
gwascentral	rs121913476
openSNP	rs121913476
23andMe	rs121913476
SNPshot	rs121913476
SNPdbe	rs121913476
MSV3d	rs121913476
GWAS Ctlg	rs121913476

Max Magnitude

0

ClinVar
Risk	rs121913476(A;A) rs121913476(G;G)
Alt	rs121913476(A;A) rs121913476(G;G)
Reference	Rs121913476(T;T)
Significance	Probable-Pathogenic
Disease	Endometrial Endometrioid Adenocarcinoma Adenocarcinoma of lung Nasopharyngeal Neoplasms Neoplasm of breast Malignant neoplasm of body of uterus
Variation	info
Gene	FGFR2
CLNDBN	Endometrial Endometrioid Adenocarcinoma, Variant with Squamous Differentiation Adenocarcinoma of lung Nasopharyngeal Neoplasms Neoplasm of breast Malignant neoplasm of body of uterus
Reversed	1
HGVS	NC_000010.10:g.123258034A>C; NC_000010.10:g.123258034A>T
CLNSRC
CLNACC	RCV000434110.1, RCV000424055.1, RCV000426965.1, RCV000433483.1, RCV000441770.1, RCV000443743.1,