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rs606231266

From SNPedia

Orientationplus
Geno Mag Summary
(CAG;CAG) 0 common in clinvar
Make rs606231266(-;-)
Make rs606231266(-;CAG)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position252420
GeneZMYND11
is asnp
is mentioned by
dbSNPrs606231266
ebirs606231266
HLIrs606231266
Exacrs606231266
Varsomers606231266
Maprs606231266
PheGenIrs606231266
hapmaprs606231266
1000 genomesrs606231266
hgdprs606231266
ensemblrs606231266
gopubmedrs606231266
geneviewrs606231266
scholarrs606231266
googlers606231266
pharmgkbrs606231266
gwascentralrs606231266
openSNPrs606231266
23andMers606231266
23andMe allrs606231266
SNP Nexus

SNPshotrs606231266
SNPdbers606231266
MSV3drs606231266
GWAS Ctlgrs606231266
Max Magnitude0
ClinVar
Risk rs606231266(;)
Alt rs606231266(;)
Reference rs606231266(CAG;CAG)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene ZMYND11
CLNDBN Mental retardation, autosomal dominant 30
Reversed 0
HGVS NC_000010.10:g.298360_298362delCAG
CLNSRC OMIM Allelic Variant
CLNACC RCV000144895.3,