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

rs121434540

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121434540(C;T)
Make rs121434540(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position89180272
GeneCDH15
is asnp
is mentioned by
dbSNPrs121434540
ebirs121434540
HLIrs121434540
Exacrs121434540
Varsomers121434540
Maprs121434540
PheGenIrs121434540
hapmaprs121434540
1000 genomesrs121434540
hgdprs121434540
ensemblrs121434540
gopubmedrs121434540
geneviewrs121434540
scholarrs121434540
googlers121434540
pharmgkbrs121434540
gwascentralrs121434540
openSNPrs121434540
23andMers121434540
23andMe allrs121434540
SNP Nexus

SNPshotrs121434540
SNPdbers121434540
MSV3drs121434540
GWAS Ctlgrs121434540
Max Magnitude0
OMIM114019
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121434540(T;T)
Alt rs121434540(T;T)
Reference rs121434540(C;C)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene CDH15
CLNDBN Mental retardation, autosomal dominant 3
Reversed 0
HGVS NC_000016.9:g.89246680C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000019210.23,