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

rs121913472

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121913472(A;A)
Make rs121913472(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position38424691
GeneFGFR1
is asnp
is mentioned by
dbSNPrs121913472
dbSNP (old)rs121913472
ClinGenrs121913472
ebirs121913472
HLIrs121913472
Exacrs121913472
Gnomadrs121913472
Varsomers121913472
Maprs121913472
PheGenIrs121913472
Biobankrs121913472
1000 genomesrs121913472
hgdprs121913472
ensemblrs121913472
gopubmedrs121913472
geneviewrs121913472
scholarrs121913472
googlers121913472
pharmgkbrs121913472
gwascentralrs121913472
openSNPrs121913472
23andMers121913472
23andMe allrs121913472
SNPshotrs121913472
SNPdbers121913472
MSV3drs121913472
GWAS Ctlgrs121913472
Max Magnitude0
ClinVar
Risk rs121913472(A;A)
Alt rs121913472(A;A)
Reference Rs121913472(C;C)
Significance Probable-Pathogenic
Disease Neoplasm
Variation info
Gene FGFR1
CLNDBN Neoplasm
Reversed 1
HGVS NC_000008.10:g.38282209G>T
CLNSRC
CLNACC RCV000436130.1,