rs1064796452

Orientation

minus

Stabilized

minus

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

Chromosome

10

Position

121515262

Gene

FGFR2

is a	snp
is	mentioned by
dbSNP	rs1064796452
dbSNP (classic)	rs1064796452
ClinGen	rs1064796452
ebi	rs1064796452
HLI	rs1064796452
Exac	rs1064796452
Gnomad	rs1064796452
Varsome	rs1064796452
LitVar	rs1064796452
Map	rs1064796452
PheGenI	rs1064796452
Biobank	rs1064796452
1000 genomes	rs1064796452
hgdp	rs1064796452
ensembl	rs1064796452
geneview	rs1064796452
scholar	rs1064796452
google	rs1064796452
pharmgkb	rs1064796452
gwascentral	rs1064796452
openSNP	rs1064796452
23andMe	rs1064796452
SNPshot	rs1064796452
SNPdbe	rs1064796452
MSV3d	rs1064796452
GWAS Ctlg	rs1064796452

Max Magnitude

0

ClinVar
Risk	rs1064796452(G;G)
Alt	rs1064796452(G;G)
Reference	Rs1064796452(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	FGFR2
CLNDBN	not provided
Reversed	1
HGVS	NC_000010.10:g.123274776T>C
CLNSRC
CLNACC	RCV000482209.1,