rs77543610

Orientation

plus

Stabilized

plus

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

Make rs77543610(C;C)

Make rs77543610(C;G)

Reference

GRCh38 38.1/141

Chromosome

10

Position

121520160

Gene

FGFR2

is a	snp
is	mentioned by
dbSNP	rs77543610
dbSNP (classic)	rs77543610
ClinGen	rs77543610
ebi	rs77543610
HLI	rs77543610
Exac	rs77543610
Gnomad	rs77543610
Varsome	rs77543610
LitVar	rs77543610
Map	rs77543610
PheGenI	rs77543610
Biobank	rs77543610
1000 genomes	rs77543610
hgdp	rs77543610
ensembl	rs77543610
geneview	rs77543610
scholar	rs77543610
google	rs77543610
pharmgkb	rs77543610
gwascentral	rs77543610
openSNP	rs77543610
23andMe	rs77543610
SNPshot	rs77543610
SNPdbe	rs77543610
MSV3d	rs77543610
GWAS Ctlg	rs77543610

Max Magnitude

0

OMIM	176943
Desc
Variant	0011
Related	also

ClinVar
Risk	rs77543610(C;C)
Alt	rs77543610(C;C)
Reference	Rs77543610(G;G)
Significance	Pathogenic
Disease	Acrocephalosyndactyly type I Head and Neck Neoplasms not provided
Variation	info
Gene	FGFR2
CLNDBN	Acrocephalosyndactyly type I Head and Neck Neoplasms not provided
Reversed	0
HGVS	NC_000010.10:g.123279674G>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000014193.24, RCV000436870.1, RCV000489611.1,