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rs1064792999

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome1
Position244054357
GeneZBTB18
is asnp
is mentioned by
dbSNPrs1064792999
dbSNP (classic)rs1064792999
ClinGenrs1064792999
ebirs1064792999
HLIrs1064792999
Exacrs1064792999
Gnomadrs1064792999
Varsomers1064792999
LitVarrs1064792999
Maprs1064792999
PheGenIrs1064792999
Biobankrs1064792999
1000 genomesrs1064792999
hgdprs1064792999
ensemblrs1064792999
geneviewrs1064792999
scholarrs1064792999
googlers1064792999
pharmgkbrs1064792999
gwascentralrs1064792999
openSNPrs1064792999
23andMers1064792999
23andMe allrs1064792999
SNPshotrs1064792999
SNPdbers1064792999
MSV3drs1064792999
GWAS Ctlgrs1064792999
Max Magnitude0
ClinVar
Risk rs1064792999(T;T)
Alt rs1064792999(T;T)
Reference Rs1064792999(C;C)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene ZBTB18
CLNDBN Mental retardation, autosomal dominant 22
Reversed 0
HGVS NC_000001.10:g.244217659C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000477670.1,