Rs121918487

Orientation

minus

is a	snp
is	mentioned by
dbSNP	rs121918487
PheGenI	rs121918487
nextbio	rs121918487
hapmap	rs121918487
1000 genomes	rs121918487
hgdp	rs121918487
ensembl	rs121918487
gopubmed	rs121918487
geneview	rs121918487
scholar	rs121918487
google	rs121918487
pharmgkb	rs121918487
gwascentral	rs121918487
openSNP	rs121918487
23andMe	rs121918487
23andMe all	rs121918487
SNP Nexus
SNPshot	rs121918487
SNPdbe	rs121918487
MSV3d	rs121918487

Gene

FGFR2

Chromosome

10

Orientation

minus

Position

123276892

Reference

GRCh37 37.1/132

Max Magnitude

0

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

Make rs121918487(A;A)

Make rs121918487(A;G)

OMIM	176943
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121918487(A;A)
Normal	rs121918487(G;G)
Significance	5
Disease	Crouzon syndrome, Pfeiffer syndrome
ClinVar	info
Gene	FGFR2
CLNDBN	Crouzon syndrome, Pfeiffer syndrome
Reversed	1
CLNHGVS	NC_000010.10:g.123276892C>T
CLNSRC	OMIM Allelic Variant