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rs875989829

From SNPedia

Orientationminus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs875989829(-;-)
Make rs875989829(-;CT)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position74741557
GeneKIAA2022
is asnp
is mentioned by
dbSNPrs875989829
ebirs875989829
HLIrs875989829
Exacrs875989829
Varsomers875989829
Maprs875989829
PheGenIrs875989829
hapmaprs875989829
1000 genomesrs875989829
hgdprs875989829
ensemblrs875989829
gopubmedrs875989829
geneviewrs875989829
scholarrs875989829
googlers875989829
pharmgkbrs875989829
gwascentralrs875989829
openSNPrs875989829
23andMers875989829
23andMe allrs875989829
SNP Nexus

SNPshotrs875989829
SNPdbers875989829
MSV3drs875989829
GWAS Ctlgrs875989829
Max Magnitude0
ClinVar
Risk rs875989829(;)
Alt rs875989829(;)
Reference rs875989829(CT;CT)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene KIAA2022
CLNDBN Mental retardation, X-linked 98
Reversed 1
HGVS NC_000023.10:g.73961392_73961393delAG
CLNSRC
CLNACC RCV000209914.3,