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rs1057519899

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057519899(A;G)
Make rs1057519899(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position38417879
GeneFGFR1
is asnp
is mentioned by
dbSNPrs1057519899
dbSNP (old)rs1057519899
ClinGenrs1057519899
ebirs1057519899
HLIrs1057519899
Exacrs1057519899
Gnomadrs1057519899
Varsomers1057519899
Maprs1057519899
PheGenIrs1057519899
Biobankrs1057519899
1000 genomesrs1057519899
hgdprs1057519899
ensemblrs1057519899
gopubmedrs1057519899
geneviewrs1057519899
scholarrs1057519899
googlers1057519899
pharmgkbrs1057519899
gwascentralrs1057519899
openSNPrs1057519899
23andMers1057519899
23andMe allrs1057519899
SNPshotrs1057519899
SNPdbers1057519899
MSV3drs1057519899
GWAS Ctlgrs1057519899
Max Magnitude0
ClinVar
Risk rs1057519899(G;G)
Alt rs1057519899(G;G)
Reference Rs1057519899(A;A)
Significance Probable-Pathogenic
Disease Medulloblastoma Adenocarcinoma of stomach Brainstem glioma Astrocytoma Neuroblastoma
Variation info
Gene FGFR1
CLNDBN Medulloblastoma Adenocarcinoma of stomach Brainstem glioma Astrocytoma Neuroblastoma
Reversed 1
HGVS NC_000008.10:g.38275397T>C
CLNSRC
CLNACC RCV000418590.1, RCV000419230.1, RCV000429290.1, RCV000435727.1, RCV000436467.1,