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rs1057519897

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519897(C;C)
Make rs1057519897(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position38414788
GeneFGFR1
is asnp
is mentioned by
dbSNPrs1057519897
dbSNP (old)rs1057519897
ClinGenrs1057519897
ebirs1057519897
HLIrs1057519897
Exacrs1057519897
Gnomadrs1057519897
Varsomers1057519897
Maprs1057519897
PheGenIrs1057519897
Biobankrs1057519897
1000 genomesrs1057519897
hgdprs1057519897
ensemblrs1057519897
gopubmedrs1057519897
geneviewrs1057519897
scholarrs1057519897
googlers1057519897
pharmgkbrs1057519897
gwascentralrs1057519897
openSNPrs1057519897
23andMers1057519897
23andMe allrs1057519897
SNPshotrs1057519897
SNPdbers1057519897
MSV3drs1057519897
GWAS Ctlgrs1057519897
Max Magnitude0
ClinVar
Risk rs1057519897(C;C)
Alt rs1057519897(C;C)
Reference Rs1057519897(G;G)
Significance Probable-Pathogenic
Disease Hepatocellular carcinoma Lymphoblastic leukemia Transitional cell carcinoma of the bladder Medulloblastoma Astrocytoma Glioblastoma
Variation info
Gene FGFR1
CLNDBN Hepatocellular carcinoma Lymphoblastic leukemia, acute, with lymphomatous features Transitional cell carcinoma of the bladder Medulloblastoma Astrocytoma Glioblastoma
Reversed 1
HGVS NC_000008.10:g.38272306C>G
CLNSRC
CLNACC RCV000422833.1, RCV000426798.1, RCV000433539.1, RCV000437662.1, RCV000443011.1, RCV000444182.1,