rs1057519898

Orientation

minus

Stabilized

minus

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

Make rs1057519898(A;G)

Make rs1057519898(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

8

Position

38417333

Gene

FGFR1

is a	snp
is	mentioned by
dbSNP	rs1057519898
dbSNP (classic)	rs1057519898
ClinGen	rs1057519898
ebi	rs1057519898
HLI	rs1057519898
Exac	rs1057519898
Gnomad	rs1057519898
Varsome	rs1057519898
LitVar	rs1057519898
Map	rs1057519898
PheGenI	rs1057519898
Biobank	rs1057519898
1000 genomes	rs1057519898
hgdp	rs1057519898
ensembl	rs1057519898
geneview	rs1057519898
scholar	rs1057519898
google	rs1057519898
pharmgkb	rs1057519898
gwascentral	rs1057519898
openSNP	rs1057519898
23andMe	rs1057519898
SNPshot	rs1057519898
SNPdbe	rs1057519898
MSV3d	rs1057519898
GWAS Ctlg	rs1057519898

Max Magnitude

0

ClinVar
Risk	rs1057519898(G;G)
Alt	rs1057519898(G;G)
Reference	Rs1057519898(A;A)
Significance	Probable-Pathogenic
Disease	Astrocytoma Neuroblastoma Brainstem glioma Medulloblastoma Adenocarcinoma of stomach
Variation	info
Gene	FGFR1
CLNDBN	Astrocytoma Neuroblastoma Brainstem glioma Medulloblastoma Adenocarcinoma of stomach
Reversed	1
HGVS	NC_000008.10:g.38274851T>C
CLNSRC
CLNACC	RCV000424432.1, RCV000425019.1, RCV000435153.1, RCV000443693.1, RCV000443832.1,