rs1057519038

Orientation

minus

Stabilized

minus

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

Make rs1057519038(A;G)

Make rs1057519038(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

10

Position

121520076

Gene

FGFR2

is a	snp
is	mentioned by
dbSNP	rs1057519038
dbSNP (classic)	rs1057519038
ClinGen	rs1057519038
ebi	rs1057519038
HLI	rs1057519038
Exac	rs1057519038
Gnomad	rs1057519038
Varsome	rs1057519038
LitVar	rs1057519038
Map	rs1057519038
PheGenI	rs1057519038
Biobank	rs1057519038
1000 genomes	rs1057519038
hgdp	rs1057519038
ensembl	rs1057519038
geneview	rs1057519038
scholar	rs1057519038
google	rs1057519038
pharmgkb	rs1057519038
gwascentral	rs1057519038
openSNP	rs1057519038
23andMe	rs1057519038
SNPshot	rs1057519038
SNPdbe	rs1057519038
MSV3d	rs1057519038
GWAS Ctlg	rs1057519038

Max Magnitude

0

ClinVar
Risk	rs1057519038(G;G)
Alt	rs1057519038(G;G)
Reference	Rs1057519038(A;A)
Significance	Probable-Pathogenic
Disease	Crouzon syndrome
Variation	info
Gene	FGFR2
CLNDBN	Crouzon syndrome
Reversed	1
HGVS	NC_000010.10:g.123279590T>C
CLNSRC
CLNACC	RCV000415488.1,