rs879253721

Orientation

minus

Stabilized

minus

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

Make rs879253721(A;G)

Make rs879253721(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

10

Position

121517316

Gene

FGFR2

is a	snp
is	mentioned by
dbSNP	rs879253721
dbSNP (classic)	rs879253721
ClinGen	rs879253721
ebi	rs879253721
HLI	rs879253721
Exac	rs879253721
Gnomad	rs879253721
Varsome	rs879253721
LitVar	rs879253721
Map	rs879253721
PheGenI	rs879253721
Biobank	rs879253721
1000 genomes	rs879253721
hgdp	rs879253721
ensembl	rs879253721
geneview	rs879253721
scholar	rs879253721
google	rs879253721
pharmgkb	rs879253721
gwascentral	rs879253721
openSNP	rs879253721
23andMe	rs879253721
SNPshot	rs879253721
SNPdbe	rs879253721
MSV3d	rs879253721
GWAS Ctlg	rs879253721

Max Magnitude

0

ClinVar
Risk	rs879253721(G;G)
Alt	rs879253721(G;G)
Reference	Rs879253721(A;A)
Significance	Pathogenic
Disease	Pfeiffer syndrome Crouzon syndrome
Variation	info
Gene	FGFR2
CLNDBN	Pfeiffer syndrome Crouzon syndrome
Reversed	1
HGVS	NC_000010.10:g.123276830T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000014225.24, RCV000014226.25,