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rs869025344

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs869025344(-;-)
Make rs869025344(-;C)
Make rs869025344(C;C)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position71300054
GeneITGB1BP2, NONO
is asnp
is mentioned by
dbSNPrs869025344
ebirs869025344
HLIrs869025344
Exacrs869025344
Varsomers869025344
Maprs869025344
PheGenIrs869025344
hapmaprs869025344
1000 genomesrs869025344
hgdprs869025344
ensemblrs869025344
gopubmedrs869025344
geneviewrs869025344
scholarrs869025344
googlers869025344
pharmgkbrs869025344
gwascentralrs869025344
openSNPrs869025344
23andMers869025344
23andMe allrs869025344
SNP Nexus

SNPshotrs869025344
SNPdbers869025344
MSV3drs869025344
GWAS Ctlgrs869025344
Max Magnitude0
ClinVar
Risk rs869025344(C;C)
Alt rs869025344(C;C)
Reference rs869025344(;)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene ITGB1BP2 NONO
CLNDBN Mental retardation, X-linked, syndromic 34
Reversed 0
HGVS NC_000023.10:g.70519904dupC
CLNSRC OMIM Allelic Variant
CLNACC RCV000207520.2,