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rs1057521724

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057521724(C;T)
Make rs1057521724(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position15946053
GeneMYCN
is asnp
is mentioned by
dbSNPrs1057521724
dbSNP (old)rs1057521724
ClinGenrs1057521724
ebirs1057521724
HLIrs1057521724
Exacrs1057521724
Gnomadrs1057521724
Varsomers1057521724
Maprs1057521724
PheGenIrs1057521724
Biobankrs1057521724
1000 genomesrs1057521724
hgdprs1057521724
ensemblrs1057521724
gopubmedrs1057521724
geneviewrs1057521724
scholarrs1057521724
googlers1057521724
pharmgkbrs1057521724
gwascentralrs1057521724
openSNPrs1057521724
23andMers1057521724
23andMe allrs1057521724
SNPshotrs1057521724
SNPdbers1057521724
MSV3drs1057521724
GWAS Ctlgrs1057521724
Max Magnitude0
ClinVar
Risk rs1057521724(T;T)
Alt rs1057521724(T;T)
Reference Rs1057521724(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYCN
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.16086175C>T
CLNSRC
CLNACC RCV000439770.1,