rs1057519036

Orientation

minus

Stabilized

minus

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

Make rs1057519036(G;G)

Make rs1057519036(G;T)

Reference

GRCh38.p7 38.3/150

Chromosome

10

Position

121520092

Gene

FGFR2

is a	snp
is	mentioned by
dbSNP	rs1057519036
dbSNP (classic)	rs1057519036
ClinGen	rs1057519036
ebi	rs1057519036
HLI	rs1057519036
Exac	rs1057519036
Gnomad	rs1057519036
Varsome	rs1057519036
LitVar	rs1057519036
Map	rs1057519036
PheGenI	rs1057519036
Biobank	rs1057519036
1000 genomes	rs1057519036
hgdp	rs1057519036
ensembl	rs1057519036
geneview	rs1057519036
scholar	rs1057519036
google	rs1057519036
pharmgkb	rs1057519036
gwascentral	rs1057519036
openSNP	rs1057519036
23andMe	rs1057519036
SNPshot	rs1057519036
SNPdbe	rs1057519036
MSV3d	rs1057519036
GWAS Ctlg	rs1057519036

Max Magnitude

0

ClinVar
Risk	rs1057519036(G;G)
Alt	rs1057519036(G;G)
Reference	Rs1057519036(T;T)
Significance	Pathogenic
Disease	Crouzon syndrome
Variation	info
Gene	FGFR2
CLNDBN	Crouzon syndrome
Reversed	1
HGVS	NC_000010.10:g.123279606A>C
CLNSRC
CLNACC	RCV000415486.1,