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rs1064794600

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(GCAGTT;GCAGTT) 0 common in clinvar
Chromosome2
Position15946060
GeneMYCN
is asnp
is mentioned by
dbSNPrs1064794600
dbSNP (old)rs1064794600
ClinGenrs1064794600
ebirs1064794600
HLIrs1064794600
Exacrs1064794600
Gnomadrs1064794600
Varsomers1064794600
Maprs1064794600
PheGenIrs1064794600
Biobankrs1064794600
1000 genomesrs1064794600
hgdprs1064794600
ensemblrs1064794600
gopubmedrs1064794600
geneviewrs1064794600
scholarrs1064794600
googlers1064794600
pharmgkbrs1064794600
gwascentralrs1064794600
openSNPrs1064794600
23andMers1064794600
23andMe allrs1064794600
SNPshotrs1064794600
SNPdbers1064794600
MSV3drs1064794600
GWAS Ctlgrs1064794600
Max Magnitude0
ClinVar
Risk rs1064794600(-;-)
Alt rs1064794600(-;-)
Reference Rs1064794600(GCAGTT;GCAGTT)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYCN
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.16086182_16086187delAGTTGC
CLNSRC
CLNACC RCV000484900.1,