Rs121434543

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Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121434543(A;T)
Make rs121434543(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position68681065
GeneCDH3
is asnp
is mentioned by
dbSNPrs121434543
Exacrs121434543
PheGenIrs121434543
nextbiors121434543
hapmaprs121434543
1000 genomesrs121434543
hgdprs121434543
ensemblrs121434543
gopubmedrs121434543
geneviewrs121434543
scholarrs121434543
googlers121434543
pharmgkbrs121434543
gwascentralrs121434543
openSNPrs121434543
23andMers121434543
23andMe allrs121434543
SNP Nexus

SNPshotrs121434543
SNPdbers121434543
MSV3drs121434543
OMIM114021
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121434543(T;T)
Alt rs121434543(T;T)
Reference rs121434543(A;A)
Significance Pathogenic
Disease EEM syndrome
Variation info
Gene CDH3
CLNDBN EEM syndrome
Reversed 0
HGVS NC_000016.9:g.68714968A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000019207.26,