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rs104893648

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104893648(A;A)
Make rs104893648(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position15945883
GeneMYCN
is asnp
is mentioned by
dbSNPrs104893648
ebirs104893648
HLIrs104893648
Exacrs104893648
Varsomers104893648
Maprs104893648
PheGenIrs104893648
hapmaprs104893648
1000 genomesrs104893648
hgdprs104893648
ensemblrs104893648
gopubmedrs104893648
geneviewrs104893648
scholarrs104893648
googlers104893648
pharmgkbrs104893648
gwascentralrs104893648
openSNPrs104893648
23andMers104893648
23andMe allrs104893648
SNP Nexus

SNPshotrs104893648
SNPdbers104893648
MSV3drs104893648
GWAS Ctlgrs104893648
Max Magnitude0
OMIM164840
Desc
Variant0003
Relatedalso
ClinVar
Risk rs104893648(A;A)
Alt rs104893648(A;A)
Reference rs104893648(G;G)
Significance Pathogenic
Disease Feingold syndrome 1
Variation info
Gene MYCN
CLNDBN Feingold syndrome 1
Reversed 0
HGVS NC_000002.11:g.16086005G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000014908.25,