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rs786205208

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205208(C;T)
Make rs786205208(T;T)
ReferenceGRCh38.p2 38.2/146
ChromosomeX
Position74742675
GeneKIAA2022
is asnp
is mentioned by
dbSNPrs786205208
ebirs786205208
HLIrs786205208
Exacrs786205208
Varsomers786205208
Maprs786205208
PheGenIrs786205208
hapmaprs786205208
1000 genomesrs786205208
hgdprs786205208
ensemblrs786205208
gopubmedrs786205208
geneviewrs786205208
scholarrs786205208
googlers786205208
pharmgkbrs786205208
gwascentralrs786205208
openSNPrs786205208
23andMers786205208
23andMe allrs786205208
SNP Nexus

SNPshotrs786205208
SNPdbers786205208
MSV3drs786205208
GWAS Ctlgrs786205208
Max Magnitude0
ClinVar
Risk rs786205208(T;T)
Alt rs786205208(T;T)
Reference rs786205208(C;C)
Significance Probable-Pathogenic
Disease Mental retardation
Variation info
Gene KIAA2022
CLNDBN Mental retardation, X-linked 98
Reversed 1
HGVS NC_000023.10:g.73962510G>A
CLNSRC
CLNACC RCV000170439.1,