Have questions? Visit https://www.reddit.com/r/SNPedia

rs606231267

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs606231267(-;-)
Make rs606231267(-;T)
Make rs606231267(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position209978
GeneZMYND11
is asnp
is mentioned by
dbSNPrs606231267
ebirs606231267
HLIrs606231267
Exacrs606231267
Varsomers606231267
Maprs606231267
PheGenIrs606231267
hapmaprs606231267
1000 genomesrs606231267
hgdprs606231267
ensemblrs606231267
gopubmedrs606231267
geneviewrs606231267
scholarrs606231267
googlers606231267
pharmgkbrs606231267
gwascentralrs606231267
openSNPrs606231267
23andMers606231267
23andMe allrs606231267
SNP Nexus

SNPshotrs606231267
SNPdbers606231267
MSV3drs606231267
GWAS Ctlgrs606231267
Max Magnitude0
ClinVar
Risk rs606231267(T;T)
Alt rs606231267(T;T)
Reference rs606231267(;)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene ZMYND11
CLNDBN Mental retardation, autosomal dominant 30
Reversed 0
HGVS NC_000010.10:g.255918dupT
CLNSRC OMIM Allelic Variant
CLNACC RCV000144896.3,