rs1057519037

Orientation

minus

Stabilized

minus

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

Make rs1057519037(GC;TA)

Make rs1057519037(TA;TA)

Reference

GRCh38.p7 38.3/150

Chromosome

10

Position

121520084

Gene

FGFR2

is a	snp
is	mentioned by
dbSNP	rs1057519037
dbSNP (classic)	rs1057519037
ClinGen	rs1057519037
ebi	rs1057519037
HLI	rs1057519037
Exac	rs1057519037
Gnomad	rs1057519037
Varsome	rs1057519037
LitVar	rs1057519037
Map	rs1057519037
PheGenI	rs1057519037
Biobank	rs1057519037
1000 genomes	rs1057519037
hgdp	rs1057519037
ensembl	rs1057519037
geneview	rs1057519037
scholar	rs1057519037
google	rs1057519037
pharmgkb	rs1057519037
gwascentral	rs1057519037
openSNP	rs1057519037
23andMe	rs1057519037
SNPshot	rs1057519037
SNPdbe	rs1057519037
MSV3d	rs1057519037
GWAS Ctlg	rs1057519037

Max Magnitude

0

ClinVar
Risk	rs1057519037(TA;TA)
Alt	rs1057519037(TA;TA)
Reference	Rs1057519037(GC;GC)
Significance	Probable-Pathogenic
Disease	Pfeiffer syndrome
Variation	info
Gene	FGFR2
CLNDBN	Pfeiffer syndrome
Reversed	1
HGVS	NC_000010.10:g.123279598_123279599delGCinsTA
CLNSRC
CLNACC	RCV000415475.1,