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rs606231268

From SNPedia

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Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs606231268(-;-)
Make rs606231268(-;GA)
Make rs606231268(GA;GA)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position248354
GeneZMYND11
is asnp
is mentioned by
dbSNPrs606231268
ebirs606231268
HLIrs606231268
Exacrs606231268
Varsomers606231268
Maprs606231268
PheGenIrs606231268
hapmaprs606231268
1000 genomesrs606231268
hgdprs606231268
ensemblrs606231268
gopubmedrs606231268
geneviewrs606231268
scholarrs606231268
googlers606231268
pharmgkbrs606231268
gwascentralrs606231268
openSNPrs606231268
23andMers606231268
23andMe allrs606231268
SNP Nexus

SNPshotrs606231268
SNPdbers606231268
MSV3drs606231268
GWAS Ctlgrs606231268
Max Magnitude0
ClinVar
Risk rs606231268(;)
Alt rs606231268(;)
Reference rs606231268(AG;AG)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene ZMYND11
CLNDBN Mental retardation, autosomal dominant 30
Reversed 0
HGVS NC_000010.10:g.294294_294295delGA
CLNSRC OMIM Allelic Variant
CLNACC RCV000144898.3,