rs869320694

Orientation

minus

Stabilized

minus

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

Make rs869320694(A;G)

Make rs869320694(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

8

Position

38414790

Gene

FGFR1

is a	snp
is	mentioned by
dbSNP	rs869320694
dbSNP (classic)	rs869320694
ClinGen	rs869320694
ebi	rs869320694
HLI	rs869320694
Exac	rs869320694
Gnomad	rs869320694
Varsome	rs869320694
LitVar	rs869320694
Map	rs869320694
PheGenI	rs869320694
Biobank	rs869320694
1000 genomes	rs869320694
hgdp	rs869320694
ensembl	rs869320694
geneview	rs869320694
scholar	rs869320694
google	rs869320694
pharmgkb	rs869320694
gwascentral	rs869320694
openSNP	rs869320694
23andMe	rs869320694
SNPshot	rs869320694
SNPdbe	rs869320694
MSV3d	rs869320694
GWAS Ctlg	rs869320694

Max Magnitude

0

ClinVar
Risk	rs869320694(G;G)
Alt	rs869320694(G;G)
Reference	Rs869320694(A;A)
Significance	Pathogenic
Disease	Encephalocraniocutaneous lipomatosis Glioblastoma Lymphoblastic leukemia Transitional cell carcinoma of the bladder Astrocytoma Hepatocellular carcinoma Medulloblastoma
Variation	info
Gene	FGFR1
CLNDBN	Encephalocraniocutaneous lipomatosis Glioblastoma Lymphoblastic leukemia, acute, with lymphomatous features Transitional cell carcinoma of the bladder Astrocytoma Hepatocellular carcinoma Medulloblastoma
Reversed	1
HGVS	NC_000008.10:g.38272308T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000210479.2, RCV000420160.1, RCV000420790.1, RCV000428027.1, RCV000430840.1, RCV000438709.1, RCV000441552.1,