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rs869025345

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869025345(C;T)
Make rs869025345(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position71297900
GeneNONO
is asnp
is mentioned by
dbSNPrs869025345
ebirs869025345
HLIrs869025345
Exacrs869025345
Varsomers869025345
Maprs869025345
PheGenIrs869025345
hapmaprs869025345
1000 genomesrs869025345
hgdprs869025345
ensemblrs869025345
gopubmedrs869025345
geneviewrs869025345
scholarrs869025345
googlers869025345
pharmgkbrs869025345
gwascentralrs869025345
openSNPrs869025345
23andMers869025345
23andMe allrs869025345
SNP Nexus

SNPshotrs869025345
SNPdbers869025345
MSV3drs869025345
GWAS Ctlgrs869025345
Max Magnitude0
ClinVar
Risk rs869025345(T;T)
Alt rs869025345(T;T)
Reference rs869025345(C;C)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene NONO
CLNDBN Mental retardation, X-linked, syndromic 34
Reversed 0
HGVS NC_000023.10:g.70517750C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000207521.1,