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rs104893636

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs104893636(A;T)
Make rs104893636(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position176151875
GeneHOXD3, HOXD4
is asnp
is mentioned by
dbSNPrs104893636
ebirs104893636
HLIrs104893636
Exacrs104893636
Varsomers104893636
Maprs104893636
PheGenIrs104893636
hapmaprs104893636
1000 genomesrs104893636
hgdprs104893636
ensemblrs104893636
gopubmedrs104893636
geneviewrs104893636
scholarrs104893636
googlers104893636
pharmgkbrs104893636
gwascentralrs104893636
openSNPrs104893636
23andMers104893636
23andMe allrs104893636
SNP Nexus

SNPshotrs104893636
SNPdbers104893636
MSV3drs104893636
GWAS Ctlgrs104893636
Max Magnitude0
OMIM142981
Desc
Variant0001
Relatedalso
ClinVar
Risk rs104893636(C,T;C,T)
Alt rs104893636(C,T;C,T)
Reference rs104893636(A;A)
Significance Other
Disease Leukemia
Variation info
Gene HOXD4 HOXD3
CLNDBN Leukemia, acute lymphoblastic, susceptibility to
Reversed 0
HGVS NC_000002.11:g.177016603A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000016017.3,