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rs398122840

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398122840(-;-)
Make rs398122840(-;G)
Make rs398122840(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position48955721
GeneBAX
is asnp
is mentioned by
dbSNPrs398122840
ebirs398122840
HLIrs398122840
Exacrs398122840
Varsomers398122840
Maprs398122840
PheGenIrs398122840
hapmaprs398122840
1000 genomesrs398122840
hgdprs398122840
ensemblrs398122840
gopubmedrs398122840
geneviewrs398122840
scholarrs398122840
googlers398122840
pharmgkbrs398122840
gwascentralrs398122840
openSNPrs398122840
23andMers398122840
23andMe allrs398122840
SNP Nexus

SNPshotrs398122840
SNPdbers398122840
MSV3drs398122840
GWAS Ctlgrs398122840
Max Magnitude0
ClinVar
Risk rs398122840(G;G)
Alt rs398122840(G;G)
Reference rs398122840(;)
Significance Pathogenic
Disease Carcinoma of colon
Variation info
Gene BAX
CLNDBN Carcinoma of colon
Reversed 0
HGVS NC_000019.9:g.49458978dupG
CLNSRC OMIM Allelic Variant
CLNACC RCV000010119.5,