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rs1057519792

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057519792(A;A)
Make rs1057519792(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position177095415
GeneFGFR4
is asnp
is mentioned by
dbSNPrs1057519792
dbSNP (old)rs1057519792
ClinGenrs1057519792
ebirs1057519792
HLIrs1057519792
Exacrs1057519792
Gnomadrs1057519792
Varsomers1057519792
Maprs1057519792
PheGenIrs1057519792
Biobankrs1057519792
1000 genomesrs1057519792
hgdprs1057519792
ensemblrs1057519792
gopubmedrs1057519792
geneviewrs1057519792
scholarrs1057519792
googlers1057519792
pharmgkbrs1057519792
gwascentralrs1057519792
openSNPrs1057519792
23andMers1057519792
23andMe allrs1057519792
SNPshotrs1057519792
SNPdbers1057519792
MSV3drs1057519792
GWAS Ctlgrs1057519792
Max Magnitude0
ClinVar
Risk rs1057519792(A;A) rs1057519792(G;G)
Alt rs1057519792(A;A) rs1057519792(G;G)
Reference Rs1057519792(C;C)
Significance Probable-Pathogenic
Disease Rhabdomyosarcoma
Variation info
Gene FGFR4
CLNDBN Rhabdomyosarcoma
Reversed 0
HGVS NC_000005.9:g.176522416C>A; NC_000005.9:g.176522416C>G
CLNSRC
CLNACC RCV000435933.1, RCV000419077.1,