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rs1057519851

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057519851(C;G)
Make rs1057519851(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position127738995
GeneMYC
is asnp
is mentioned by
dbSNPrs1057519851
dbSNP (classic)rs1057519851
ClinGenrs1057519851
ebirs1057519851
HLIrs1057519851
Exacrs1057519851
Gnomadrs1057519851
Varsomers1057519851
LitVarrs1057519851
Maprs1057519851
PheGenIrs1057519851
Biobankrs1057519851
1000 genomesrs1057519851
hgdprs1057519851
ensemblrs1057519851
geneviewrs1057519851
scholarrs1057519851
googlers1057519851
pharmgkbrs1057519851
gwascentralrs1057519851
openSNPrs1057519851
23andMers1057519851
23andMe allrs1057519851
SNPshotrs1057519851
SNPdbers1057519851
MSV3drs1057519851
GWAS Ctlgrs1057519851
Max Magnitude0
ClinVar
Risk rs1057519851(G;G)
Alt rs1057519851(G;G)
Reference Rs1057519851(C;C)
Significance Probable-Pathogenic
Disease Neoplasm
Variation info
Gene MYC
CLNDBN Neoplasm
Reversed 0
HGVS NC_000008.10:g.128751241C>G
CLNSRC
CLNACC RCV000444724.1,