rs1057520536

Orientation

minus

Stabilized

minus

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

Make rs1057520536(C;G)

Make rs1057520536(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

8

Position

38414186

Gene

FGFR1

is a	snp
is	mentioned by
dbSNP	rs1057520536
dbSNP (classic)	rs1057520536
ClinGen	rs1057520536
ebi	rs1057520536
HLI	rs1057520536
Exac	rs1057520536
Gnomad	rs1057520536
Varsome	rs1057520536
LitVar	rs1057520536
Map	rs1057520536
PheGenI	rs1057520536
Biobank	rs1057520536
1000 genomes	rs1057520536
hgdp	rs1057520536
ensembl	rs1057520536
geneview	rs1057520536
scholar	rs1057520536
google	rs1057520536
pharmgkb	rs1057520536
gwascentral	rs1057520536
openSNP	rs1057520536
23andMe	rs1057520536
SNPshot	rs1057520536
SNPdbe	rs1057520536
MSV3d	rs1057520536
GWAS Ctlg	rs1057520536

Max Magnitude

0

ClinVar
Risk	rs1057520536(G;G)
Alt	rs1057520536(G;G)
Reference	Rs1057520536(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	FGFR1
CLNDBN	not provided
Reversed	1
HGVS	NC_000008.10:g.38271704G>C
CLNSRC
CLNACC	RCV000423621.1,