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rs104893856

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs104893856(A;A)
Make rs104893856(A;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position41746162
GenePHOX2B
is asnp
is mentioned by
dbSNPrs104893856
ebirs104893856
HLIrs104893856
Exacrs104893856
Varsomers104893856
Maprs104893856
PheGenIrs104893856
hapmaprs104893856
1000 genomesrs104893856
hgdprs104893856
ensemblrs104893856
gopubmedrs104893856
geneviewrs104893856
scholarrs104893856
googlers104893856
pharmgkbrs104893856
gwascentralrs104893856
openSNPrs104893856
23andMers104893856
23andMe allrs104893856
SNP Nexus

SNPshotrs104893856
SNPdbers104893856
MSV3drs104893856
GWAS Ctlgrs104893856
Max Magnitude0
OMIM603851
Desc
Variant0008
Relatedalso
ClinVar
Risk rs104893856(A;A)
Alt rs104893856(A;A)
Reference rs104893856(G;G)
Significance Other
Disease Neuroblastoma 2
Variation info
Gene PHOX2B
CLNDBN Neuroblastoma 2
Reversed 1
HGVS NC_000004.11:g.41748179C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006385.2,