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rs398122513

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398122513(A;A)
Make rs398122513(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position48955799
GeneBAX
is asnp
is mentioned by
dbSNPrs398122513
ebirs398122513
HLIrs398122513
Exacrs398122513
Varsomers398122513
Maprs398122513
PheGenIrs398122513
hapmaprs398122513
1000 genomesrs398122513
hgdprs398122513
ensemblrs398122513
gopubmedrs398122513
geneviewrs398122513
scholarrs398122513
googlers398122513
pharmgkbrs398122513
gwascentralrs398122513
openSNPrs398122513
23andMers398122513
23andMe allrs398122513
SNP Nexus

SNPshotrs398122513
SNPdbers398122513
MSV3drs398122513
GWAS Ctlgrs398122513
Max Magnitude0
ClinVar
Risk rs398122513(A;A)
Alt rs398122513(A;A)
Reference rs398122513(G;G)
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.49459056G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010121.4,