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rs121913473

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121913473(C;T)
Make rs121913473(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position38428420
GeneFGFR1
is asnp
is mentioned by
dbSNPrs121913473
dbSNP (old)rs121913473
ClinGenrs121913473
ebirs121913473
HLIrs121913473
Exacrs121913473
Gnomadrs121913473
Varsomers121913473
Maprs121913473
PheGenIrs121913473
Biobankrs121913473
1000 genomesrs121913473
hgdprs121913473
ensemblrs121913473
gopubmedrs121913473
geneviewrs121913473
scholarrs121913473
googlers121913473
pharmgkbrs121913473
gwascentralrs121913473
openSNPrs121913473
23andMers121913473
23andMe allrs121913473
SNPshotrs121913473
SNPdbers121913473
MSV3drs121913473
GWAS Ctlgrs121913473
Max Magnitude0
ClinVar
Risk rs121913473(T;T)
Alt rs121913473(T;T)
Reference Rs121913473(C;C)
Significance Probable-Pathogenic
Disease Neoplasm
Variation info
Gene FGFR1
CLNDBN Neoplasm
Reversed 1
HGVS NC_000008.10:g.38285938G>A
CLNSRC
CLNACC RCV000418895.1,