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rs1057519918

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057519918(C;T)
Make rs1057519918(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position127738390
GeneMYC
is asnp
is mentioned by
dbSNPrs1057519918
dbSNP (old)rs1057519918
ClinGenrs1057519918
ebirs1057519918
HLIrs1057519918
Exacrs1057519918
Gnomadrs1057519918
Varsomers1057519918
Maprs1057519918
PheGenIrs1057519918
Biobankrs1057519918
1000 genomesrs1057519918
hgdprs1057519918
ensemblrs1057519918
gopubmedrs1057519918
geneviewrs1057519918
scholarrs1057519918
googlers1057519918
pharmgkbrs1057519918
gwascentralrs1057519918
openSNPrs1057519918
23andMers1057519918
23andMe allrs1057519918
SNPshotrs1057519918
SNPdbers1057519918
MSV3drs1057519918
GWAS Ctlgrs1057519918
Max Magnitude0
ClinVar
Risk rs1057519918(T;T)
Alt rs1057519918(T;T)
Reference Rs1057519918(C;C)
Significance Probable-Pathogenic
Disease Malignant lymphoma Adenocarcinoma of lung Oesophageal carcinoma Neuroblastoma Malignant melanoma of skin
Variation info
Gene MYC
CLNDBN Malignant lymphoma, non-Hodgkin Adenocarcinoma of lung Oesophageal carcinoma Neuroblastoma Malignant melanoma of skin
Reversed 0
HGVS NC_000008.10:g.128750636C>T
CLNSRC
CLNACC RCV000418915.1, RCV000427867.1, RCV000428982.1, RCV000436178.1, RCV000438593.1,