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rs121913480

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913480(G;T)
Make rs121913480(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome4
Position1806604
GeneFGFR3
is asnp
is mentioned by
dbSNPrs121913480
dbSNP (classic)rs121913480
ClinGenrs121913480
ebirs121913480
HLIrs121913480
Exacrs121913480
Gnomadrs121913480
Varsomers121913480
LitVarrs121913480
Maprs121913480
PheGenIrs121913480
Biobankrs121913480
1000 genomesrs121913480
hgdprs121913480
ensemblrs121913480
geneviewrs121913480
scholarrs121913480
googlers121913480
pharmgkbrs121913480
gwascentralrs121913480
openSNPrs121913480
23andMers121913480
SNPshotrs121913480
SNPdbers121913480
MSV3drs121913480
GWAS Ctlgrs121913480
Max Magnitude0
ClinVar
Risk rs121913480(T;T)
Alt rs121913480(T;T)
Reference Rs121913480(G;G)
Significance Probable-Pathogenic
Disease Bladder carcinoma Carcinoma
Variation info
Gene FGFR3
CLNDBN Bladder carcinoma Carcinoma
Reversed 0
HGVS NC_000004.11:g.1808331G>T
CLNSRC
CLNACC RCV000417814.1, RCV000440614.1,