rs1057519897

Orientation

minus

Stabilized

minus

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

Make rs1057519897(C;C)

Make rs1057519897(C;G)

Reference

GRCh38.p7 38.3/150

Chromosome

8

Position

38414788

Gene

FGFR1

is a	snp
is	mentioned by
dbSNP	rs1057519897
dbSNP (classic)	rs1057519897
ClinGen	rs1057519897
ebi	rs1057519897
HLI	rs1057519897
Exac	rs1057519897
Gnomad	rs1057519897
Varsome	rs1057519897
LitVar	rs1057519897
Map	rs1057519897
PheGenI	rs1057519897
Biobank	rs1057519897
1000 genomes	rs1057519897
hgdp	rs1057519897
ensembl	rs1057519897
geneview	rs1057519897
scholar	rs1057519897
google	rs1057519897
pharmgkb	rs1057519897
gwascentral	rs1057519897
openSNP	rs1057519897
23andMe	rs1057519897
SNPshot	rs1057519897
SNPdbe	rs1057519897
MSV3d	rs1057519897
GWAS Ctlg	rs1057519897

Max Magnitude

0

ClinVar
Risk	rs1057519897(C;C)
Alt	rs1057519897(C;C)
Reference	Rs1057519897(G;G)
Significance	Probable-Pathogenic
Disease	Hepatocellular carcinoma Lymphoblastic leukemia Transitional cell carcinoma of the bladder Medulloblastoma Astrocytoma Glioblastoma
Variation	info
Gene	FGFR1
CLNDBN	Hepatocellular carcinoma Lymphoblastic leukemia, acute, with lymphomatous features Transitional cell carcinoma of the bladder Medulloblastoma Astrocytoma Glioblastoma
Reversed	1
HGVS	NC_000008.10:g.38272306C>G
CLNSRC
CLNACC	RCV000422833.1, RCV000426798.1, RCV000433539.1, RCV000437662.1, RCV000443011.1, RCV000444182.1,