rs121913473

Orientation

minus

Stabilized

minus

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

Make rs121913473(C;T)

Make rs121913473(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

8

Position

38428420

Gene

FGFR1

is a	snp
is	mentioned by
dbSNP	rs121913473
dbSNP (classic)	rs121913473
ClinGen	rs121913473
ebi	rs121913473
HLI	rs121913473
Exac	rs121913473
Gnomad	rs121913473
Varsome	rs121913473
LitVar	rs121913473
Map	rs121913473
PheGenI	rs121913473
Biobank	rs121913473
1000 genomes	rs121913473
hgdp	rs121913473
ensembl	rs121913473
geneview	rs121913473
scholar	rs121913473
google	rs121913473
pharmgkb	rs121913473
gwascentral	rs121913473
openSNP	rs121913473
23andMe	rs121913473
SNPshot	rs121913473
SNPdbe	rs121913473
MSV3d	rs121913473
GWAS Ctlg	rs121913473

Max Magnitude

0

ClinVar
Risk	rs121913473(T;T)
Alt	rs121913473(T;T)
Reference	Rs121913473(C;C)
Significance	Probable-Pathogenic
Disease	Neoplasm
Variation	info
Gene	FGFR1
CLNDBN	Neoplasm
Reversed	1
HGVS	NC_000008.10:g.38285938G>A
CLNSRC
CLNACC	RCV000418895.1,