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rs1060505032

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060505032(-;-)
Make rs1060505032(-;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position85271596
GeneZNF711
is asnp
is mentioned by
dbSNPrs1060505032
dbSNP (old)rs1060505032
ClinGenrs1060505032
ebirs1060505032
HLIrs1060505032
Exacrs1060505032
Gnomadrs1060505032
Varsomers1060505032
LitVarrs1060505032
Maprs1060505032
PheGenIrs1060505032
Biobankrs1060505032
1000 genomesrs1060505032
hgdprs1060505032
ensemblrs1060505032
gopubmedrs1060505032
geneviewrs1060505032
scholarrs1060505032
googlers1060505032
pharmgkbrs1060505032
gwascentralrs1060505032
openSNPrs1060505032
23andMers1060505032
23andMe allrs1060505032
SNPshotrs1060505032
SNPdbers1060505032
MSV3drs1060505032
GWAS Ctlgrs1060505032
Max Magnitude0
ClinVar
Risk rs1060505032(-;-)
Alt rs1060505032(-;-)
Reference Rs1060505032(T;T)
Significance Pathogenic
Disease ZNF711-Related X-linked Mental Retardation
Variation info
Gene ZNF711
CLNDBN ZNF711-Related X-linked Mental Retardation
Reversed 0
HGVS NC_000023.10:g.84526602delT
CLNSRC OMIM Allelic Variant
CLNACC RCV000477669.1,