Have questions? Visit https://www.reddit.com/r/SNPedia

rs121913111

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913111(A;A)
Make rs121913111(A;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position1803725
GeneFGFR3
is asnp
is mentioned by
dbSNPrs121913111
ebirs121913111
HLIrs121913111
Exacrs121913111
Varsomers121913111
Maprs121913111
PheGenIrs121913111
hapmaprs121913111
1000 genomesrs121913111
hgdprs121913111
ensemblrs121913111
gopubmedrs121913111
geneviewrs121913111
scholarrs121913111
googlers121913111
pharmgkbrs121913111
gwascentralrs121913111
openSNPrs121913111
23andMers121913111
23andMe allrs121913111
SNP Nexus

SNPshotrs121913111
SNPdbers121913111
MSV3drs121913111
GWAS Ctlgrs121913111
Max Magnitude0
OMIM134934
Desc
Variant0025
Relatedalso
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
CLNACC RCV000017761.5,