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rs121918368

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121918368(C;T)
Make rs121918368(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position3150939
GeneCRBN
is asnp
is mentioned by
dbSNPrs121918368
ebirs121918368
HLIrs121918368
Exacrs121918368
Varsomers121918368
Maprs121918368
PheGenIrs121918368
hapmaprs121918368
1000 genomesrs121918368
hgdprs121918368
ensemblrs121918368
gopubmedrs121918368
geneviewrs121918368
scholarrs121918368
googlers121918368
pharmgkbrs121918368
gwascentralrs121918368
openSNPrs121918368
23andMers121918368
23andMe allrs121918368
SNP Nexus

SNPshotrs121918368
SNPdbers121918368
MSV3drs121918368
GWAS Ctlgrs121918368
Max Magnitude0
OMIM609262
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121918368(T;T)
Alt rs121918368(T;T)
Reference rs121918368(C;C)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene CRBN
CLNDBN Mental retardation, autosomal recessive 2
Reversed 1
HGVS NC_000003.11:g.3192623G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000001895.3,



[PMID 26521987] Polymorphisms within beta-catenin encoding gene affect multiple myeloma development and treatment