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

rs587776836

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587776836(-;-)
Make rs587776836(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position1801945
GeneFGFR3
is asnp
is mentioned by
dbSNPrs587776836
ebirs587776836
HLIrs587776836
Exacrs587776836
Varsomers587776836
Maprs587776836
PheGenIrs587776836
hapmaprs587776836
1000 genomesrs587776836
hgdprs587776836
ensemblrs587776836
gopubmedrs587776836
geneviewrs587776836
scholarrs587776836
googlers587776836
pharmgkbrs587776836
gwascentralrs587776836
openSNPrs587776836
23andMers587776836
23andMe allrs587776836
SNP Nexus

SNPshotrs587776836
SNPdbers587776836
MSV3drs587776836
GWAS Ctlgrs587776836
Max Magnitude0
ClinVar
Risk rs587776836(;)
Alt rs587776836(;)
Reference rs587776836(C;C)
Significance Pathogenic
Disease Carcinoma of colon
Variation info
Gene FGFR3
CLNDBN Carcinoma of colon
Reversed 0
HGVS NC_000004.11:g.1803672delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000017762.5,