rs121913479

Orientation

plus

Stabilized

plus

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

Make rs121913479(G;T)

Make rs121913479(T;T)

Reference

GRCh38 38.1/141

Chromosome

4

Position

1804362

Gene

FGFR3

is a	snp
is	mentioned by
dbSNP	rs121913479
dbSNP (classic)	rs121913479
ClinGen	rs121913479
ebi	rs121913479
HLI	rs121913479
Exac	rs121913479
Gnomad	rs121913479
Varsome	rs121913479
LitVar	rs121913479
Map	rs121913479
PheGenI	rs121913479
Biobank	rs121913479
1000 genomes	rs121913479
hgdp	rs121913479
ensembl	rs121913479
geneview	rs121913479
scholar	rs121913479
google	rs121913479
pharmgkb	rs121913479
gwascentral	rs121913479
openSNP	rs121913479
23andMe	rs121913479
SNPshot	rs121913479
SNPdbe	rs121913479
MSV3d	rs121913479
GWAS Ctlg	rs121913479

Max Magnitude

0

OMIM	134934
Desc
Variant	0033
Related	also

ClinVar
Risk	rs121913479(T;T)
Alt	rs121913479(T;T)
Reference	Rs121913479(G;G)
Significance	Pathogenic
Disease	Thanatophoric dysplasia type 1 Epidermal nevus not provided Bladder carcinoma
Variation	info
Gene	FGFR3
CLNDBN	Thanatophoric dysplasia type 1 Epidermal nevus not provided Bladder carcinoma
Reversed	0
HGVS	NC_000004.11:g.1806089G>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000017770.28, RCV000029208.5, RCV000413645.1, RCV000443051.1,