rs1057519041

Orientation

minus

Stabilized

minus

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

Make rs1057519041(A;G)

Make rs1057519041(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

10

Position

121517465

Gene

FGFR2

is a	snp
is	mentioned by
dbSNP	rs1057519041
dbSNP (classic)	rs1057519041
ClinGen	rs1057519041
ebi	rs1057519041
HLI	rs1057519041
Exac	rs1057519041
Gnomad	rs1057519041
Varsome	rs1057519041
LitVar	rs1057519041
Map	rs1057519041
PheGenI	rs1057519041
Biobank	rs1057519041
1000 genomes	rs1057519041
hgdp	rs1057519041
ensembl	rs1057519041
geneview	rs1057519041
scholar	rs1057519041
google	rs1057519041
pharmgkb	rs1057519041
gwascentral	rs1057519041
openSNP	rs1057519041
23andMe	rs1057519041
SNPshot	rs1057519041
SNPdbe	rs1057519041
MSV3d	rs1057519041
GWAS Ctlg	rs1057519041

Max Magnitude

0

ClinVar
Risk	rs1057519041(G;G)
Alt	rs1057519041(G;G)
Reference	Rs1057519041(A;A)
Significance	Pathogenic
Disease	Pfeiffer syndrome
Variation	info
Gene	FGFR2
CLNDBN	Pfeiffer syndrome
Reversed	1
HGVS	NC_000010.10:g.123276979T>C
CLNSRC
CLNACC	RCV000415479.1,