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rs1060505033

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060505033(C;C)
Make rs1060505033(C;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position85264383
GeneZNF711
is asnp
is mentioned by
dbSNPrs1060505033
dbSNP (old)rs1060505033
ClinGenrs1060505033
ebirs1060505033
HLIrs1060505033
Exacrs1060505033
Gnomadrs1060505033
Varsomers1060505033
LitVarrs1060505033
Maprs1060505033
PheGenIrs1060505033
Biobankrs1060505033
1000 genomesrs1060505033
hgdprs1060505033
ensemblrs1060505033
gopubmedrs1060505033
geneviewrs1060505033
scholarrs1060505033
googlers1060505033
pharmgkbrs1060505033
gwascentralrs1060505033
openSNPrs1060505033
23andMers1060505033
23andMe allrs1060505033
SNPshotrs1060505033
SNPdbers1060505033
MSV3drs1060505033
GWAS Ctlgrs1060505033
Max Magnitude0
ClinVar
Risk rs1060505033(C;C)
Alt rs1060505033(C;C)
Reference Rs1060505033(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.84519389T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000477705.1,