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rs527236035

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs527236035(A;G)
Make rs527236035(G;G)
ReferenceGRCh38 38.1/142
Chromosome6
Position131591361
GeneMED23
is asnp
is mentioned by
dbSNPrs527236035
ebirs527236035
HLIrs527236035
Exacrs527236035
Varsomers527236035
Maprs527236035
PheGenIrs527236035
hapmaprs527236035
1000 genomesrs527236035
hgdprs527236035
ensemblrs527236035
gopubmedrs527236035
geneviewrs527236035
scholarrs527236035
googlers527236035
pharmgkbrs527236035
gwascentralrs527236035
openSNPrs527236035
23andMers527236035
23andMe allrs527236035
SNP Nexus

SNPshotrs527236035
SNPdbers527236035
MSV3drs527236035
GWAS Ctlgrs527236035
Max Magnitude0
ClinVar
Risk rs527236035(G;G)
Alt rs527236035(G;G)
Reference rs527236035(A;A)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene MED23
CLNDBN Mental retardation, autosomal recessive 18
Reversed 1
HGVS NC_000006.11:g.131912501T>C
CLNSRC ClinVar
CLNACC RCV000132726.1,