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

rs672601341

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs672601341(-;-)
Make rs672601341(-;G)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position237629
GeneZMYND11
is asnp
is mentioned by
dbSNPrs672601341
ebirs672601341
HLIrs672601341
Exacrs672601341
Varsomers672601341
Maprs672601341
PheGenIrs672601341
hapmaprs672601341
1000 genomesrs672601341
hgdprs672601341
ensemblrs672601341
gopubmedrs672601341
geneviewrs672601341
scholarrs672601341
googlers672601341
pharmgkbrs672601341
gwascentralrs672601341
openSNPrs672601341
23andMers672601341
23andMe allrs672601341
SNP Nexus

SNPshotrs672601341
SNPdbers672601341
MSV3drs672601341
GWAS Ctlgrs672601341
Max Magnitude0
ClinVar
Risk rs672601341(;)
Alt rs672601341(;)
Reference rs672601341(G;G)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene ZMYND11
CLNDBN Mental retardation, autosomal dominant 30
Reversed 0
HGVS NC_000010.10:g.283569delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000144899.3,