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rs398122842

From SNPedia

Orientationplus
Geno Mag Summary
(GGGGGGG;GGGGGGG) 0 common in clinvar
Make rs398122842(-;-)
Make rs398122842(-;GGGGGGG)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position48955715
GeneBAX
is asnp
is mentioned by
dbSNPrs398122842
ebirs398122842
HLIrs398122842
Exacrs398122842
Varsomers398122842
Maprs398122842
PheGenIrs398122842
hapmaprs398122842
1000 genomesrs398122842
hgdprs398122842
ensemblrs398122842
gopubmedrs398122842
geneviewrs398122842
scholarrs398122842
googlers398122842
pharmgkbrs398122842
gwascentralrs398122842
openSNPrs398122842
23andMers398122842
23andMe allrs398122842
SNP Nexus

SNPshotrs398122842
SNPdbers398122842
MSV3drs398122842
GWAS Ctlgrs398122842
Max Magnitude0
ClinVar
Risk rs398122842(;)
Alt rs398122842(;)
Reference rs398122842(GGGGGGG;GGGGGGG)
Significance Pathogenic
Disease T-cell acute lymphoblastic leukemia
Variation info
Gene BAX
CLNDBN T-cell acute lymphoblastic leukemia
Reversed 0
HGVS NC_000019.9:g.49458972_49458978delGGGGGGG
CLNSRC OMIM Allelic Variant
CLNACC RCV000010122.5,