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rs1057519898

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057519898(A;G)
Make rs1057519898(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position38417333
GeneFGFR1
is asnp
is mentioned by
dbSNPrs1057519898
dbSNP (old)rs1057519898
ClinGenrs1057519898
ebirs1057519898
HLIrs1057519898
Exacrs1057519898
Gnomadrs1057519898
Varsomers1057519898
Maprs1057519898
PheGenIrs1057519898
Biobankrs1057519898
1000 genomesrs1057519898
hgdprs1057519898
ensemblrs1057519898
gopubmedrs1057519898
geneviewrs1057519898
scholarrs1057519898
googlers1057519898
pharmgkbrs1057519898
gwascentralrs1057519898
openSNPrs1057519898
23andMers1057519898
23andMe allrs1057519898
SNPshotrs1057519898
SNPdbers1057519898
MSV3drs1057519898
GWAS Ctlgrs1057519898
Max Magnitude0
ClinVar
Risk rs1057519898(G;G)
Alt rs1057519898(G;G)
Reference Rs1057519898(A;A)
Significance Probable-Pathogenic
Disease Astrocytoma Neuroblastoma Brainstem glioma Medulloblastoma Adenocarcinoma of stomach
Variation info
Gene FGFR1
CLNDBN Astrocytoma Neuroblastoma Brainstem glioma Medulloblastoma Adenocarcinoma of stomach
Reversed 1
HGVS NC_000008.10:g.38274851T>C
CLNSRC
CLNACC RCV000424432.1, RCV000425019.1, RCV000435153.1, RCV000443693.1, RCV000443832.1,