Rs121434541

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Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121434541(C;T)
Make rs121434541(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position89183555
GeneCDH15
is asnp
is mentioned by
dbSNPrs121434541
Exacrs121434541
PheGenIrs121434541
nextbiors121434541
hapmaprs121434541
1000 genomesrs121434541
hgdprs121434541
ensemblrs121434541
gopubmedrs121434541
geneviewrs121434541
scholarrs121434541
googlers121434541
pharmgkbrs121434541
gwascentralrs121434541
openSNPrs121434541
23andMers121434541
23andMe allrs121434541
SNP Nexus

SNPshotrs121434541
SNPdbers121434541
MSV3drs121434541
GMAF0.0
Max Magnitude0
OMIM114019
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121434541(T;T)
Alt rs121434541(T;T)
Reference rs121434541(C;C)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene CDH15
CLNDBN Mental retardation, autosomal dominant 3
Reversed 0
HGVS NC_000016.9:g.89249963C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000019211.26,