rs121913111

Orientation

plus

Stabilized

plus

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

Make rs121913111(A;A)

Make rs121913111(A;G)

Reference

GRCh38 38.1/141

Chromosome

4

Position

1803725

Gene

FGFR3

is a	snp
is	mentioned by
dbSNP	rs121913111
dbSNP (classic)	rs121913111
ClinGen	rs121913111
ebi	rs121913111
HLI	rs121913111
Exac	rs121913111
Gnomad	rs121913111
Varsome	rs121913111
LitVar	rs121913111
Map	rs121913111
PheGenI	rs121913111
Biobank	rs121913111
1000 genomes	rs121913111
hgdp	rs121913111
ensembl	rs121913111
geneview	rs121913111
scholar	rs121913111
google	rs121913111
pharmgkb	rs121913111
gwascentral	rs121913111
openSNP	rs121913111
23andMe	rs121913111
SNPshot	rs121913111
SNPdbe	rs121913111
MSV3d	rs121913111
GWAS Ctlg	rs121913111

Max Magnitude

0

OMIM	134934
Desc
Variant	0025
Related	also

ClinVar
Risk	rs121913111(A;A)
Alt	rs121913111(A;A)
Reference	Rs121913111(G;G)
Significance	Pathogenic
Disease	Carcinoma of colon
Variation	info
Gene	FGFR3
CLNDBN	Carcinoma of colon
Reversed	0
HGVS	NC_000004.11:g.1805452G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000017761.5,