Have questions? Visit https://www.reddit.com/r/SNPedia

rs1060499655

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060499655(-;-)
Make rs1060499655(-;C)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position244054373
GeneZBTB18
is asnp
is mentioned by
dbSNPrs1060499655
dbSNP (classic)rs1060499655
ClinGenrs1060499655
ebirs1060499655
HLIrs1060499655
Exacrs1060499655
Gnomadrs1060499655
Varsomers1060499655
LitVarrs1060499655
Maprs1060499655
PheGenIrs1060499655
Biobankrs1060499655
1000 genomesrs1060499655
hgdprs1060499655
ensemblrs1060499655
geneviewrs1060499655
scholarrs1060499655
googlers1060499655
pharmgkbrs1060499655
gwascentralrs1060499655
openSNPrs1060499655
23andMers1060499655
23andMe allrs1060499655
SNPshotrs1060499655
SNPdbers1060499655
MSV3drs1060499655
GWAS Ctlgrs1060499655
Max Magnitude0
ClinVar
Risk rs1060499655(-;-)
Alt rs1060499655(-;-)
Reference Rs1060499655(C;C)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene ZBTB18
CLNDBN Mental retardation, autosomal dominant 22
Reversed 0
HGVS NC_000001.10:g.244217675delC
CLNSRC
CLNACC RCV000449542.1,