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rs398122406

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398122406(G;T)
Make rs398122406(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position244054171
GeneZBTB18
is asnp
is mentioned by
dbSNPrs398122406
ebirs398122406
HLIrs398122406
Exacrs398122406
Varsomers398122406
Maprs398122406
PheGenIrs398122406
hapmaprs398122406
1000 genomesrs398122406
hgdprs398122406
ensemblrs398122406
gopubmedrs398122406
geneviewrs398122406
scholarrs398122406
googlers398122406
pharmgkbrs398122406
gwascentralrs398122406
openSNPrs398122406
23andMers398122406
23andMe allrs398122406
SNP Nexus

SNPshotrs398122406
SNPdbers398122406
MSV3drs398122406
GWAS Ctlgrs398122406
Max Magnitude0
ClinVar
Risk rs398122406(T;T)
Alt rs398122406(T;T)
Reference rs398122406(G;G)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene ZBTB18
CLNDBN Mental retardation, autosomal dominant 22
Reversed 0
HGVS NC_000001.10:g.244217473G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000074444.5,