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rs121913666

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913666(A;A)
Make rs121913666(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position15945847
GeneMYCN
is asnp
is mentioned by
dbSNPrs121913666
ebirs121913666
HLIrs121913666
Exacrs121913666
Varsomers121913666
Maprs121913666
PheGenIrs121913666
hapmaprs121913666
1000 genomesrs121913666
hgdprs121913666
ensemblrs121913666
gopubmedrs121913666
geneviewrs121913666
scholarrs121913666
googlers121913666
pharmgkbrs121913666
gwascentralrs121913666
openSNPrs121913666
23andMers121913666
23andMe allrs121913666
SNP Nexus

SNPshotrs121913666
SNPdbers121913666
MSV3drs121913666
GWAS Ctlgrs121913666
Max Magnitude0
OMIM164840
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121913666(A;A)
Alt rs121913666(A;A)
Reference rs121913666(G;G)
Significance Pathogenic
Disease Feingold syndrome 1
Variation info
Gene MYCN
CLNDBN Feingold syndrome 1
Reversed 0
HGVS NC_000002.11:g.16085969G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000014912.21,