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rs1060499652

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060499652(A;A)
Make rs1060499652(A;C)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position74741087
GeneKIAA2022
is asnp
is mentioned by
dbSNPrs1060499652
dbSNP (old)rs1060499652
ClinGenrs1060499652
ebirs1060499652
HLIrs1060499652
Exacrs1060499652
Gnomadrs1060499652
Varsomers1060499652
Maprs1060499652
PheGenIrs1060499652
Biobankrs1060499652
1000 genomesrs1060499652
hgdprs1060499652
ensemblrs1060499652
gopubmedrs1060499652
geneviewrs1060499652
scholarrs1060499652
googlers1060499652
pharmgkbrs1060499652
gwascentralrs1060499652
openSNPrs1060499652
23andMers1060499652
23andMe allrs1060499652
SNPshotrs1060499652
SNPdbers1060499652
MSV3drs1060499652
GWAS Ctlgrs1060499652
Max Magnitude0
ClinVar
Risk rs1060499652(A;A)
Alt rs1060499652(A;A)
Reference Rs1060499652(C;C)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene KIAA2022
CLNDBN Mental retardation, X-linked 98
Reversed 1
HGVS NC_000023.10:g.73960922G>T
CLNSRC
CLNACC RCV000449555.1,