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rs1057519919

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057519919(C;T)
Make rs1057519919(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position15942195
GeneMYCN, MYCNOS
is asnp
is mentioned by
dbSNPrs1057519919
dbSNP (old)rs1057519919
ClinGenrs1057519919
ebirs1057519919
HLIrs1057519919
Exacrs1057519919
Gnomadrs1057519919
Varsomers1057519919
Maprs1057519919
PheGenIrs1057519919
Biobankrs1057519919
1000 genomesrs1057519919
hgdprs1057519919
ensemblrs1057519919
gopubmedrs1057519919
geneviewrs1057519919
scholarrs1057519919
googlers1057519919
pharmgkbrs1057519919
gwascentralrs1057519919
openSNPrs1057519919
23andMers1057519919
23andMe allrs1057519919
SNPshotrs1057519919
SNPdbers1057519919
MSV3drs1057519919
GWAS Ctlgrs1057519919
Max Magnitude0
ClinVar
Risk rs1057519919(T;T)
Alt rs1057519919(T;T)
Reference Rs1057519919(C;C)
Significance Probable-Pathogenic
Disease Malignant neoplasm of body of uterus Glioblastoma Pancreatic adenocarcinoma Neuroblastoma Medulloblastoma
Variation info
Gene MYCN MYCNOS
CLNDBN Malignant neoplasm of body of uterus Glioblastoma Pancreatic adenocarcinoma Neuroblastoma Medulloblastoma
Reversed 0
HGVS NC_000002.11:g.16082317C>T
CLNSRC
CLNACC RCV000421370.1, RCV000423772.1, RCV000428589.1, RCV000434477.1, RCV000441008.1,