rs1057518060

Orientation

minus

Stabilized

minus

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

Make rs1057518060(C;C)

Make rs1057518060(C;G)

Reference

GRCh38.p7 38.3/150

Chromosome

8

Position

38414276

Gene

FGFR1

is a	snp
is	mentioned by
dbSNP	rs1057518060
dbSNP (classic)	rs1057518060
ClinGen	rs1057518060
ebi	rs1057518060
HLI	rs1057518060
Exac	rs1057518060
Gnomad	rs1057518060
Varsome	rs1057518060
LitVar	rs1057518060
Map	rs1057518060
PheGenI	rs1057518060
Biobank	rs1057518060
1000 genomes	rs1057518060
hgdp	rs1057518060
ensembl	rs1057518060
geneview	rs1057518060
scholar	rs1057518060
google	rs1057518060
pharmgkb	rs1057518060
gwascentral	rs1057518060
openSNP	rs1057518060
23andMe	rs1057518060
SNPshot	rs1057518060
SNPdbe	rs1057518060
MSV3d	rs1057518060
GWAS Ctlg	rs1057518060

Max Magnitude

0

ClinVar
Risk	rs1057518060(C;C)
Alt	rs1057518060(C;C)
Reference	Rs1057518060(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	FGFR1
CLNDBN	not provided
Reversed	1
HGVS	NC_000008.10:g.38271794C>G
CLNSRC
CLNACC	RCV000413066.1,