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rs727503977

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs727503977(-;-)
Make rs727503977(-;A)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position74742975
GeneKIAA2022
is asnp
is mentioned by
dbSNPrs727503977
ebirs727503977
HLIrs727503977
Exacrs727503977
Varsomers727503977
Maprs727503977
PheGenIrs727503977
hapmaprs727503977
1000 genomesrs727503977
hgdprs727503977
ensemblrs727503977
gopubmedrs727503977
geneviewrs727503977
scholarrs727503977
googlers727503977
pharmgkbrs727503977
gwascentralrs727503977
openSNPrs727503977
23andMers727503977
23andMe allrs727503977
SNP Nexus

SNPshotrs727503977
SNPdbers727503977
MSV3drs727503977
GWAS Ctlgrs727503977
Max Magnitude0
ClinVar
Risk rs727503977(;)
Alt rs727503977(;)
Reference rs727503977(A;A)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene KIAA2022
CLNDBN Mental retardation, X-linked 98
Reversed 1
HGVS NC_000023.10:g.73962810delT
CLNSRC
CLNACC RCV000153401.3,