rs387906678

Orientation

minus

Stabilized

minus

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

Make rs387906678(G;G)

Make rs387906678(G;T)

Reference

GRCh38 38.1/141

Chromosome

10

Position

121515263

Gene

FGFR2

is a	snp
is	mentioned by
dbSNP	rs387906678
dbSNP (classic)	rs387906678
ClinGen	rs387906678
ebi	rs387906678
HLI	rs387906678
Exac	rs387906678
Gnomad	rs387906678
Varsome	rs387906678
LitVar	rs387906678
Map	rs387906678
PheGenI	rs387906678
Biobank	rs387906678
1000 genomes	rs387906678
hgdp	rs387906678
ensembl	rs387906678
geneview	rs387906678
scholar	rs387906678
google	rs387906678
pharmgkb	rs387906678
gwascentral	rs387906678
openSNP	rs387906678
23andMe	rs387906678
SNPshot	rs387906678
SNPdbe	rs387906678
MSV3d	rs387906678
GWAS Ctlg	rs387906678

Max Magnitude

0

ClinVar
Risk	rs387906678(C;C) rs387906678(G;G)
Alt	rs387906678(C;C) rs387906678(G;G)
Reference	Rs387906678(T;T)
Significance	Pathogenic
Disease	Bent bone dysplasia syndrome Inborn genetic diseases Oesophageal carcinoma Endometrial neoplasm Malignant neoplasm of body of uterus Adenocarcinoma of stomach
Variation	info
Gene	FGFR2
CLNDBN	Bent bone dysplasia syndrome Inborn genetic diseases Oesophageal carcinoma Endometrial neoplasm Malignant neoplasm of body of uterus Adenocarcinoma of stomach
Reversed	1
HGVS	NC_000010.10:g.123274777A>C; NC_000010.10:g.123274777A>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000022735.25, RCV000190765.1, RCV000424046.1, RCV000427294.1, RCV000430563.1, RCV000441347.1,