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rs587777135

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CAA;CAA) 0 common in clinvar
(TTGG;TTGG) 0 common in clinvar
Make rs587777135(-;-)
Make rs587777135(-;CAA)
ReferenceGRCh38 38.1/142
Chromosome10
Position65966714
GeneCTNNA3
is asnp
is mentioned by
dbSNPrs587777135
ebirs587777135
HLIrs587777135
Exacrs587777135
Varsomers587777135
Maprs587777135
PheGenIrs587777135
hapmaprs587777135
1000 genomesrs587777135
hgdprs587777135
ensemblrs587777135
gopubmedrs587777135
geneviewrs587777135
scholarrs587777135
googlers587777135
pharmgkbrs587777135
gwascentralrs587777135
openSNPrs587777135
23andMers587777135
23andMe allrs587777135
SNP Nexus

SNPshotrs587777135
SNPdbers587777135
MSV3drs587777135
GWAS Ctlgrs587777135
Max Magnitude0
ClinVar
Risk rs587777135(CAAG,G;CAAG,G)
Alt rs587777135(CAAG,G;CAAG,G)
Reference rs587777135(TTGG;TTGG)
Significance Pathogenic
Disease Arrhythmogenic right ventricular dysplasia
Variation info
Gene CTNNA3
CLNDBN Arrhythmogenic right ventricular dysplasia, familial, 13
Reversed 1
HGVS NC_000010.10:g.67726472_67726474delCAA
CLNSRC OMIM Allelic Variant
CLNACC RCV000087057.3,