rs1057519042

Orientation

minus

Stabilized

minus

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

Make rs1057519042(A;G)

Make rs1057519042(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

10

Position

121517396

Gene

FGFR2

is a	snp
is	mentioned by
dbSNP	rs1057519042
dbSNP (classic)	rs1057519042
ClinGen	rs1057519042
ebi	rs1057519042
HLI	rs1057519042
Exac	rs1057519042
Gnomad	rs1057519042
Varsome	rs1057519042
LitVar	rs1057519042
Map	rs1057519042
PheGenI	rs1057519042
Biobank	rs1057519042
1000 genomes	rs1057519042
hgdp	rs1057519042
ensembl	rs1057519042
geneview	rs1057519042
scholar	rs1057519042
google	rs1057519042
pharmgkb	rs1057519042
gwascentral	rs1057519042
openSNP	rs1057519042
23andMe	rs1057519042
SNPshot	rs1057519042
SNPdbe	rs1057519042
MSV3d	rs1057519042
GWAS Ctlg	rs1057519042

Max Magnitude

0

ClinVar
Risk	rs1057519042(G;G)
Alt	rs1057519042(G;G)
Reference	Rs1057519042(A;A)
Significance	Pathogenic
Disease	Crouzon syndrome
Variation	info
Gene	FGFR2
CLNDBN	Crouzon syndrome
Reversed	1
HGVS	NC_000010.10:g.123276910T>C
CLNSRC
CLNACC	RCV000415483.1,