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rs869320713

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869320713(A;A)
Make rs869320713(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position248370
GeneZMYND11
is asnp
is mentioned by
dbSNPrs869320713
ebirs869320713
HLIrs869320713
Exacrs869320713
Varsomers869320713
Maprs869320713
PheGenIrs869320713
hapmaprs869320713
1000 genomesrs869320713
hgdprs869320713
ensemblrs869320713
gopubmedrs869320713
geneviewrs869320713
scholarrs869320713
googlers869320713
pharmgkbrs869320713
gwascentralrs869320713
openSNPrs869320713
23andMers869320713
23andMe allrs869320713
SNP Nexus

SNPshotrs869320713
SNPdbers869320713
MSV3drs869320713
GWAS Ctlgrs869320713
Max Magnitude0
ClinVar
Risk rs869320713(A;A)
Alt rs869320713(A;A)
Reference rs869320713(G;G)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene ZMYND11
CLNDBN Mental retardation, autosomal dominant 30
Reversed 0
HGVS NC_000010.10:g.294310G>A
CLNSRC
CLNACC RCV000210880.1,