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rs121913667

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913667(A;A)
Make rs121913667(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position15942295
GeneMYCN
is asnp
is mentioned by
dbSNPrs121913667
ebirs121913667
HLIrs121913667
Exacrs121913667
Varsomers121913667
Maprs121913667
PheGenIrs121913667
hapmaprs121913667
1000 genomesrs121913667
hgdprs121913667
ensemblrs121913667
gopubmedrs121913667
geneviewrs121913667
scholarrs121913667
googlers121913667
pharmgkbrs121913667
gwascentralrs121913667
openSNPrs121913667
23andMers121913667
23andMe allrs121913667
SNP Nexus

SNPshotrs121913667
SNPdbers121913667
MSV3drs121913667
GWAS Ctlgrs121913667
Max Magnitude0
OMIM164840
Desc
Variant0007
Relatedalso
ClinVar
Risk rs121913667(A;A)
Alt rs121913667(A;A)
Reference rs121913667(G;G)
Significance Pathogenic
Disease Feingold syndrome 1
Variation info
Gene MYCN MYCNOS
CLNDBN Feingold syndrome 1
Reversed 0
HGVS NC_000002.11:g.16082417G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000014909.25,