Have questions? Visit https://www.reddit.com/r/SNPedia

rs869025343

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869025343(A;A)
Make rs869025343(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position71297938
GeneNONO
is asnp
is mentioned by
dbSNPrs869025343
dbSNP (old)rs869025343
ClinGenrs869025343
ebirs869025343
HLIrs869025343
Exacrs869025343
Gnomadrs869025343
Varsomers869025343
Maprs869025343
PheGenIrs869025343
Biobankrs869025343
1000 genomesrs869025343
hgdprs869025343
ensemblrs869025343
gopubmedrs869025343
geneviewrs869025343
scholarrs869025343
googlers869025343
pharmgkbrs869025343
gwascentralrs869025343
openSNPrs869025343
23andMers869025343
23andMe allrs869025343
SNP Nexus

SNPshotrs869025343
SNPdbers869025343
MSV3drs869025343
GWAS Ctlgrs869025343
Max Magnitude0
ClinVar
Risk rs869025343(A;A)
Alt rs869025343(A;A)
Reference Rs869025343(G;G)
Significance Pathogenic
Disease Mental retardation not provided
Variation info
Gene NONO
CLNDBN Mental retardation, X-linked, syndromic 34 not provided
Reversed 0
HGVS NC_000023.10:g.70517788G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000207522.3, RCV000306159.1,