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rs398122800

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398122800(-;-)
Make rs398122800(-;A)
Make rs398122800(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position201209189
GeneCASP10
is asnp
is mentioned by
dbSNPrs398122800
ebirs398122800
HLIrs398122800
Exacrs398122800
Varsomers398122800
Maprs398122800
PheGenIrs398122800
hapmaprs398122800
1000 genomesrs398122800
hgdprs398122800
ensemblrs398122800
gopubmedrs398122800
geneviewrs398122800
scholarrs398122800
googlers398122800
pharmgkbrs398122800
gwascentralrs398122800
openSNPrs398122800
23andMers398122800
23andMe allrs398122800
SNP Nexus

SNPshotrs398122800
SNPdbers398122800
MSV3drs398122800
GWAS Ctlgrs398122800
Max Magnitude0
ClinVar
Risk rs398122800(A;A)
Alt rs398122800(A;A)
Reference rs398122800(;)
Significance Pathogenic
Disease Malignant lymphoma
Variation info
Gene CASP10
CLNDBN Malignant lymphoma, non-Hodgkin
Reversed 0
HGVS NC_000002.11:g.202073912_202073913insA
CLNSRC OMIM Allelic Variant
CLNACC RCV000008209.4,