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rs104893646

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104893646(A;A)
Make rs104893646(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position15945880
GeneMYCN
is asnp
is mentioned by
dbSNPrs104893646
ebirs104893646
HLIrs104893646
Exacrs104893646
Varsomers104893646
Maprs104893646
PheGenIrs104893646
hapmaprs104893646
1000 genomesrs104893646
hgdprs104893646
ensemblrs104893646
gopubmedrs104893646
geneviewrs104893646
scholarrs104893646
googlers104893646
pharmgkbrs104893646
gwascentralrs104893646
openSNPrs104893646
23andMers104893646
23andMe allrs104893646
SNP Nexus

SNPshotrs104893646
SNPdbers104893646
MSV3drs104893646
GWAS Ctlgrs104893646
Max Magnitude0
OMIM164840
Desc
Variant0001
Relatedalso
ClinVar
Risk rs104893646(A;A)
Alt rs104893646(A;A)
Reference rs104893646(G;G)
Significance Pathogenic
Disease Feingold syndrome 1
Variation info
Gene MYCN
CLNDBN Feingold syndrome 1
Reversed 0
HGVS NC_000002.11:g.16086002G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000014906.25,