rs121913485

Orientation

plus

Stabilized

plus

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

Make rs121913485(A;G)

Make rs121913485(G;G)

Reference

GRCh38 38.1/141

Chromosome

4

Position

1804372

Gene

FGFR3

is a	snp
is	mentioned by
dbSNP	rs121913485
dbSNP (classic)	rs121913485
ClinGen	rs121913485
ebi	rs121913485
HLI	rs121913485
Exac	rs121913485
Gnomad	rs121913485
Varsome	rs121913485
LitVar	rs121913485
Map	rs121913485
PheGenI	rs121913485
Biobank	rs121913485
1000 genomes	rs121913485
hgdp	rs121913485
ensembl	rs121913485
geneview	rs121913485
scholar	rs121913485
google	rs121913485
pharmgkb	rs121913485
gwascentral	rs121913485
openSNP	rs121913485
23andMe	rs121913485
SNPshot	rs121913485
SNPdbe	rs121913485
MSV3d	rs121913485
GWAS Ctlg	rs121913485

Max Magnitude

0

OMIM	134934
Desc
Variant	0016
Related	also

ClinVar
Risk	rs121913485(G;G)
Alt	rs121913485(G;G)
Reference	Rs121913485(A;A)
Significance	Pathogenic
Disease	Thanatophoric dysplasia type 1 not provided Carcinoma Myeloproliferative disorder Papillary renal cell carcinoma Transitional cell carcinoma of the bladder Bladder carcinoma
Variation	info
Gene	FGFR3
CLNDBN	Thanatophoric dysplasia type 1 not provided Carcinoma Myeloproliferative disorder Papillary renal cell carcinoma, sporadic Transitional cell carcinoma of the bladder Bladder carcinoma
Reversed	0
HGVS	NC_000004.11:g.1806099A>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000017751.24, RCV000255235.2, RCV000419796.1, RCV000421104.1, RCV000427428.1, RCV000434824.1, RCV000442248.1,