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rs797045036

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs797045036(C;C)
Make rs797045036(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position3151023
GeneCRBN, TRNT1
is asnp
is mentioned by
dbSNPrs797045036
ebirs797045036
HLIrs797045036
Exacrs797045036
Varsomers797045036
Maprs797045036
PheGenIrs797045036
hapmaprs797045036
1000 genomesrs797045036
hgdprs797045036
ensemblrs797045036
gopubmedrs797045036
geneviewrs797045036
scholarrs797045036
googlers797045036
pharmgkbrs797045036
gwascentralrs797045036
openSNPrs797045036
23andMers797045036
23andMe allrs797045036
SNP Nexus

SNPshotrs797045036
SNPdbers797045036
MSV3drs797045036
GWAS Ctlgrs797045036
Max Magnitude0
ClinVar
Risk rs797045036(C;C)
Alt rs797045036(C;C)
Reference rs797045036(T;T)
Significance Probable-Pathogenic
Disease Mental retardation
Variation info
Gene CRBN
CLNDBN Mental retardation, autosomal recessive 2
Reversed 1
HGVS NC_000003.11:g.3192707A>G
CLNSRC Baylor College of Medicine
CLNACC RCV000191075.1,