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rs113994115

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs113994115(G;T)
Make rs113994115(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position15942281
GeneMYCN, MYCNOS
is asnp
is mentioned by
dbSNPrs113994115
ebirs113994115
HLIrs113994115
Exacrs113994115
Varsomers113994115
Maprs113994115
PheGenIrs113994115
hapmaprs113994115
1000 genomesrs113994115
hgdprs113994115
ensemblrs113994115
gopubmedrs113994115
geneviewrs113994115
scholarrs113994115
googlers113994115
pharmgkbrs113994115
gwascentralrs113994115
openSNPrs113994115
23andMers113994115
23andMe allrs113994115
SNP Nexus

SNPshotrs113994115
SNPdbers113994115
MSV3drs113994115
GWAS Ctlgrs113994115
Max Magnitude0
OMIM164840
Desc
Variant0004
Relatedalso
ClinVar
Risk rs113994115(T;T)
Alt rs113994115(T;T)
Reference rs113994115(G;G)
Significance Pathogenic
Disease Feingold syndrome 1
Variation info
Gene MYCN MYCNOS
CLNDBN Feingold syndrome 1
Reversed 0
HGVS NC_000002.11:g.16082403G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000014910.25,