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rs28936699

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs28936699(C;T)
Make rs28936699(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position201209388
GeneCASP10
is asnp
is mentioned by
dbSNPrs28936699
dbSNP (classic)rs28936699
ClinGenrs28936699
ebirs28936699
HLIrs28936699
Exacrs28936699
Gnomadrs28936699
Varsomers28936699
LitVarrs28936699
Maprs28936699
PheGenIrs28936699
Biobankrs28936699
1000 genomesrs28936699
hgdprs28936699
ensemblrs28936699
geneviewrs28936699
scholarrs28936699
googlers28936699
pharmgkbrs28936699
gwascentralrs28936699
openSNPrs28936699
23andMers28936699
23andMe allrs28936699
SNPshotrs28936699
SNPdbers28936699
MSV3drs28936699
GWAS Ctlgrs28936699
Max Magnitude0

NOTE: the OMIM entry cited below refers to a somatic mutation, not a germline SNP

OMIM601762
DescNON-HODGKIN LYMPHOMA, SOMATIC
Variant0003
Relatedalso



ClinVar
Risk rs28936699(T;T)
Alt rs28936699(T;T)
Reference Rs28936699(C;C)
Significance Pathogenic
Disease Malignant lymphoma
Variation info
Gene CASP10
CLNDBN Malignant lymphoma, non-Hodgkin
Reversed 0
HGVS NC_000002.11:g.202074111C>T
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000008206.5,