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rs1057518728

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057518728(-;T)
Make rs1057518728(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position74740308
GeneKIAA2022
is asnp
is mentioned by
dbSNPrs1057518728
dbSNP (old)rs1057518728
ClinGenrs1057518728
ebirs1057518728
HLIrs1057518728
Exacrs1057518728
Gnomadrs1057518728
Varsomers1057518728
Maprs1057518728
PheGenIrs1057518728
Biobankrs1057518728
1000 genomesrs1057518728
hgdprs1057518728
ensemblrs1057518728
gopubmedrs1057518728
geneviewrs1057518728
scholarrs1057518728
googlers1057518728
pharmgkbrs1057518728
gwascentralrs1057518728
openSNPrs1057518728
23andMers1057518728
23andMe allrs1057518728
SNPshotrs1057518728
SNPdbers1057518728
MSV3drs1057518728
GWAS Ctlgrs1057518728
Max Magnitude0
ClinVar
Risk rs1057518728(T;T)
Alt rs1057518728(T;T)
Reference Rs1057518728(-;-)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene KIAA2022
CLNDBN Mental retardation, X-linked 98
Reversed 1
HGVS NC_000023.10:g.73960144dupA
CLNSRC
CLNACC RCV000415267.1,