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rs876661316

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876661316(G;T)
Make rs876661316(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position71298509
GeneNONO
is asnp
is mentioned by
dbSNPrs876661316
ebirs876661316
HLIrs876661316
Exacrs876661316
Varsomers876661316
Maprs876661316
PheGenIrs876661316
hapmaprs876661316
1000 genomesrs876661316
hgdprs876661316
ensemblrs876661316
gopubmedrs876661316
geneviewrs876661316
scholarrs876661316
googlers876661316
pharmgkbrs876661316
gwascentralrs876661316
openSNPrs876661316
23andMers876661316
23andMe allrs876661316
SNP Nexus

SNPshotrs876661316
SNPdbers876661316
MSV3drs876661316
GWAS Ctlgrs876661316
Max Magnitude0
ClinVar
Risk rs876661316(T;T)
Alt rs876661316(T;T)
Reference rs876661316(G;G)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene NONO
CLNDBN Mental retardation, X-linked, syndromic 34
Reversed 0
HGVS NC_000023.10:g.70518359G>T
CLNSRC
CLNACC RCV000223722.1,