rs1057519899

Orientation

minus

Stabilized

minus

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

Make rs1057519899(A;G)

Make rs1057519899(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

8

Position

38417879

Gene

FGFR1

is a	snp
is	mentioned by
dbSNP	rs1057519899
dbSNP (classic)	rs1057519899
ClinGen	rs1057519899
ebi	rs1057519899
HLI	rs1057519899
Exac	rs1057519899
Gnomad	rs1057519899
Varsome	rs1057519899
LitVar	rs1057519899
Map	rs1057519899
PheGenI	rs1057519899
Biobank	rs1057519899
1000 genomes	rs1057519899
hgdp	rs1057519899
ensembl	rs1057519899
geneview	rs1057519899
scholar	rs1057519899
google	rs1057519899
pharmgkb	rs1057519899
gwascentral	rs1057519899
openSNP	rs1057519899
23andMe	rs1057519899
SNPshot	rs1057519899
SNPdbe	rs1057519899
MSV3d	rs1057519899
GWAS Ctlg	rs1057519899

Max Magnitude

0

ClinVar
Risk	rs1057519899(G;G)
Alt	rs1057519899(G;G)
Reference	Rs1057519899(A;A)
Significance	Probable-Pathogenic
Disease	Medulloblastoma Adenocarcinoma of stomach Brainstem glioma Astrocytoma Neuroblastoma
Variation	info
Gene	FGFR1
CLNDBN	Medulloblastoma Adenocarcinoma of stomach Brainstem glioma Astrocytoma Neuroblastoma
Reversed	1
HGVS	NC_000008.10:g.38275397T>C
CLNSRC
CLNACC	RCV000418590.1, RCV000419230.1, RCV000429290.1, RCV000435727.1, RCV000436467.1,