Have questions? Visit https://www.reddit.com/r/SNPedia

rs398122841

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398122841(-;-)
Make rs398122841(-;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position48955721
GeneBAX
is asnp
is mentioned by
dbSNPrs398122841
ebirs398122841
HLIrs398122841
Exacrs398122841
Varsomers398122841
Maprs398122841
PheGenIrs398122841
hapmaprs398122841
1000 genomesrs398122841
hgdprs398122841
ensemblrs398122841
gopubmedrs398122841
geneviewrs398122841
scholarrs398122841
googlers398122841
pharmgkbrs398122841
gwascentralrs398122841
openSNPrs398122841
23andMers398122841
23andMe allrs398122841
SNP Nexus

SNPshotrs398122841
SNPdbers398122841
MSV3drs398122841
GWAS Ctlgrs398122841
Max Magnitude0
ClinVar
Risk rs398122841(;)
Alt rs398122841(;)
Reference rs398122841(G;G)
Significance Pathogenic
Disease Carcinoma of colon
Variation info
Gene BAX
CLNDBN Carcinoma of colon
Reversed 0
HGVS NC_000019.9:g.49458978delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000010120.5,