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rs527236036

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs527236036(C;T)
Make rs527236036(T;T)
ReferenceGRCh38 38.1/142
Chromosome6
Position131587798
GeneMED23
is asnp
is mentioned by
dbSNPrs527236036
ebirs527236036
HLIrs527236036
Exacrs527236036
Varsomers527236036
Maprs527236036
PheGenIrs527236036
hapmaprs527236036
1000 genomesrs527236036
hgdprs527236036
ensemblrs527236036
gopubmedrs527236036
geneviewrs527236036
scholarrs527236036
googlers527236036
pharmgkbrs527236036
gwascentralrs527236036
openSNPrs527236036
23andMers527236036
23andMe allrs527236036
SNP Nexus

SNPshotrs527236036
SNPdbers527236036
MSV3drs527236036
GWAS Ctlgrs527236036
Max Magnitude0
ClinVar
Risk rs527236036(T;T)
Alt rs527236036(T;T)
Reference rs527236036(C;C)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene MED23
CLNDBN Mental retardation, autosomal recessive 18
Reversed 1
HGVS NC_000006.11:g.131908938G>A
CLNSRC ClinVar
CLNACC RCV000132727.1,