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rs387906350

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs387906350(-;-)
Make rs387906350(-;T)
Make rs387906350(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position85267829
GeneBCL10
is asnp
is mentioned by
dbSNPrs387906350
ebirs387906350
HLIrs387906350
Exacrs387906350
Varsomers387906350
Maprs387906350
PheGenIrs387906350
hapmaprs387906350
1000 genomesrs387906350
hgdprs387906350
ensemblrs387906350
gopubmedrs387906350
geneviewrs387906350
scholarrs387906350
googlers387906350
pharmgkbrs387906350
gwascentralrs387906350
openSNPrs387906350
23andMers387906350
23andMe allrs387906350
SNP Nexus

SNPshotrs387906350
SNPdbers387906350
MSV3drs387906350
GWAS Ctlgrs387906350
Max Magnitude0
ClinVar
Risk rs387906350(T;T)
Alt rs387906350(T;T)
Reference rs387906350(;)
Significance Pathogenic
Disease Mucosa-associated lymphoma Mesothelioma Male germ cell tumor
Variation info
Gene BCL10
CLNDBN Mucosa-associated lymphoma Mesothelioma Male germ cell tumor, somatic
Reversed 1
HGVS NC_000001.10:g.85733513dupA
CLNSRC OMIM Allelic Variant
CLNACC RCV000006628.4, RCV000023306.4, RCV000023307.4,