rs1057520044

Orientation

minus

Stabilized

minus

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

Make rs1057520044(A;G)

Make rs1057520044(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

10

Position

121498597

Gene

FGFR2

is a	snp
is	mentioned by
dbSNP	rs1057520044
dbSNP (classic)	rs1057520044
ClinGen	rs1057520044
ebi	rs1057520044
HLI	rs1057520044
Exac	rs1057520044
Gnomad	rs1057520044
Varsome	rs1057520044
LitVar	rs1057520044
Map	rs1057520044
PheGenI	rs1057520044
Biobank	rs1057520044
1000 genomes	rs1057520044
hgdp	rs1057520044
ensembl	rs1057520044
geneview	rs1057520044
scholar	rs1057520044
google	rs1057520044
pharmgkb	rs1057520044
gwascentral	rs1057520044
openSNP	rs1057520044
23andMe	rs1057520044
SNPshot	rs1057520044
SNPdbe	rs1057520044
MSV3d	rs1057520044
GWAS Ctlg	rs1057520044

Max Magnitude

0

ClinVar
Risk	rs1057520044(G;G)
Alt	rs1057520044(G;G)
Reference	Rs1057520044(A;A)
Significance	Probable-Pathogenic
Disease	Craniosynostosis syndrome
Variation	info
Gene	FGFR2
CLNDBN	Craniosynostosis syndrome
Reversed	1
HGVS	NC_000010.10:g.123258111T>C
CLNSRC
CLNACC	RCV000424161.1,