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rs121908981

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs121908981(C;G)
Make rs121908981(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position1898251
GeneMAD1L1
is asnp
is mentioned by
dbSNPrs121908981
ebirs121908981
HLIrs121908981
Exacrs121908981
Varsomers121908981
Maprs121908981
PheGenIrs121908981
hapmaprs121908981
1000 genomesrs121908981
hgdprs121908981
ensemblrs121908981
gopubmedrs121908981
geneviewrs121908981
scholarrs121908981
googlers121908981
pharmgkbrs121908981
gwascentralrs121908981
openSNPrs121908981
23andMers121908981
23andMe allrs121908981
SNP Nexus

SNPshotrs121908981
SNPdbers121908981
MSV3drs121908981
GWAS Ctlgrs121908981
Max Magnitude0
OMIM602686
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121908981(G;G)
Alt rs121908981(G;G)
Reference rs121908981(C;C)
Significance Pathogenic
Disease Lymphoma
Variation info
Gene MAD1L1
CLNDBN Lymphoma, somatic
Reversed 1
HGVS NC_000007.13:g.1937887G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000007328.4,