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rs104893855

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs104893855(G;T)
Make rs104893855(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position41747479
GenePHOX2B
is asnp
is mentioned by
dbSNPrs104893855
ebirs104893855
HLIrs104893855
Exacrs104893855
Varsomers104893855
Maprs104893855
PheGenIrs104893855
hapmaprs104893855
1000 genomesrs104893855
hgdprs104893855
ensemblrs104893855
gopubmedrs104893855
geneviewrs104893855
scholarrs104893855
googlers104893855
pharmgkbrs104893855
gwascentralrs104893855
openSNPrs104893855
23andMers104893855
23andMe allrs104893855
SNP Nexus

SNPshotrs104893855
SNPdbers104893855
MSV3drs104893855
GWAS Ctlgrs104893855
Max Magnitude0
OMIM603851
Desc
Variant0005
Relatedalso
ClinVar
Risk rs104893855(T;T)
Alt rs104893855(T;T)
Reference rs104893855(G;G)
Significance Other
Disease Neuroblastoma 2
Variation info
Gene PHOX2B
CLNDBN Neuroblastoma 2
Reversed 1
HGVS NC_000004.11:g.41749496C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000006382.3,