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rs1057519850

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057519850(C;T)
Make rs1057519850(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position127738447
GeneMYC
is asnp
is mentioned by
dbSNPrs1057519850
dbSNP (old)rs1057519850
ClinGenrs1057519850
ebirs1057519850
HLIrs1057519850
Exacrs1057519850
Gnomadrs1057519850
Varsomers1057519850
LitVarrs1057519850
Maprs1057519850
PheGenIrs1057519850
Biobankrs1057519850
1000 genomesrs1057519850
hgdprs1057519850
ensemblrs1057519850
gopubmedrs1057519850
geneviewrs1057519850
scholarrs1057519850
googlers1057519850
pharmgkbrs1057519850
gwascentralrs1057519850
openSNPrs1057519850
23andMers1057519850
23andMe allrs1057519850
SNPshotrs1057519850
SNPdbers1057519850
MSV3drs1057519850
GWAS Ctlgrs1057519850
Max Magnitude0
ClinVar
Risk rs1057519850(T;T)
Alt rs1057519850(T;T)
Reference Rs1057519850(C;C)
Significance Probable-Pathogenic
Disease Neoplasm
Variation info
Gene MYC
CLNDBN Neoplasm
Reversed 0
HGVS NC_000008.10:g.128750693C>T
CLNSRC
CLNACC RCV000424357.1,