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rs1057517770

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057517770(C;T)
Make rs1057517770(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position15945894
GeneMYCN
is asnp
is mentioned by
dbSNPrs1057517770
dbSNP (classic)rs1057517770
ClinGenrs1057517770
ebirs1057517770
HLIrs1057517770
Exacrs1057517770
Gnomadrs1057517770
Varsomers1057517770
LitVarrs1057517770
Maprs1057517770
PheGenIrs1057517770
Biobankrs1057517770
1000 genomesrs1057517770
hgdprs1057517770
ensemblrs1057517770
geneviewrs1057517770
scholarrs1057517770
googlers1057517770
pharmgkbrs1057517770
gwascentralrs1057517770
openSNPrs1057517770
23andMers1057517770
23andMe allrs1057517770
SNPshotrs1057517770
SNPdbers1057517770
MSV3drs1057517770
GWAS Ctlgrs1057517770
Max Magnitude0
ClinVar
Risk rs1057517770(T;T)
Alt rs1057517770(T;T)
Reference Rs1057517770(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYCN
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.16086016C>T
CLNSRC
CLNACC RCV000414637.1,