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rs370667926

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs370667926(C;T)
Make rs370667926(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position131603129
GeneMED23
is asnp
is mentioned by
dbSNPrs370667926
ebirs370667926
HLIrs370667926
Exacrs370667926
Varsomers370667926
Maprs370667926
PheGenIrs370667926
hapmaprs370667926
1000 genomesrs370667926
hgdprs370667926
ensemblrs370667926
gopubmedrs370667926
geneviewrs370667926
scholarrs370667926
googlers370667926
pharmgkbrs370667926
gwascentralrs370667926
openSNPrs370667926
23andMers370667926
23andMe allrs370667926
SNP Nexus

SNPshotrs370667926
SNPdbers370667926
MSV3drs370667926
GWAS Ctlgrs370667926
Max Magnitude0
ClinVar
Risk rs370667926(T;T)
Alt rs370667926(T;T)
Reference rs370667926(C;C)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene MED23
CLNDBN Mental retardation, autosomal recessive 18
Reversed 0
HGVS NC_000006.11:g.131924269C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000023395.2,