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rs1057519849

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057519849(C;T)
Make rs1057519849(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position127738386
GeneMYC
is asnp
is mentioned by
dbSNPrs1057519849
dbSNP (old)rs1057519849
ClinGenrs1057519849
ebirs1057519849
HLIrs1057519849
Exacrs1057519849
Gnomadrs1057519849
Varsomers1057519849
LitVarrs1057519849
Maprs1057519849
PheGenIrs1057519849
Biobankrs1057519849
1000 genomesrs1057519849
hgdprs1057519849
ensemblrs1057519849
gopubmedrs1057519849
geneviewrs1057519849
scholarrs1057519849
googlers1057519849
pharmgkbrs1057519849
gwascentralrs1057519849
openSNPrs1057519849
23andMers1057519849
23andMe allrs1057519849
SNPshotrs1057519849
SNPdbers1057519849
MSV3drs1057519849
GWAS Ctlgrs1057519849
Max Magnitude0
ClinVar
Risk rs1057519849(T;T)
Alt rs1057519849(T;T)
Reference Rs1057519849(C;C)
Significance Probable-Pathogenic
Disease Neoplasm
Variation info
Gene MYC
CLNDBN Neoplasm
Reversed 0
HGVS NC_000008.10:g.128750632C>T
CLNSRC
CLNACC RCV000429575.1,