rs387906676

Orientation

minus

Stabilized

minus

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

Make rs387906676(C;C)

Make rs387906676(C;G)

Reference

GRCh38 38.1/141

Chromosome

10

Position

121517394

Gene

FGFR2

is a	snp
is	mentioned by
dbSNP	rs387906676
dbSNP (classic)	rs387906676
ClinGen	rs387906676
ebi	rs387906676
HLI	rs387906676
Exac	rs387906676
Gnomad	rs387906676
Varsome	rs387906676
LitVar	rs387906676
Map	rs387906676
PheGenI	rs387906676
Biobank	rs387906676
1000 genomes	rs387906676
hgdp	rs387906676
ensembl	rs387906676
geneview	rs387906676
scholar	rs387906676
google	rs387906676
pharmgkb	rs387906676
gwascentral	rs387906676
openSNP	rs387906676
23andMe	rs387906676
SNPshot	rs387906676
SNPdbe	rs387906676
MSV3d	rs387906676
GWAS Ctlg	rs387906676

Max Magnitude

0

ClinVar
Risk	rs387906676(A;A) rs387906676(C;C)
Alt	rs387906676(A;A) rs387906676(C;C)
Reference	Rs387906676(G;G)
Significance	Pathogenic
Disease	Crouzon syndrome Variant of unknown significance
Variation	info
Gene	FGFR2
CLNDBN	Crouzon syndrome Variant of unknown significance
Reversed	1
HGVS	NC_000010.10:g.123276908C>G; NC_000010.10:g.123276908C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000022732.25, RCV000022733.3,