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

rs151010429

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151010429(A;A)
Make rs151010429(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position14130828
GeneTMEM43
is asnp
is mentioned by
dbSNPrs151010429
ebirs151010429
HLIrs151010429
Exacrs151010429
Varsomers151010429
Maprs151010429
PheGenIrs151010429
hapmaprs151010429
1000 genomesrs151010429
hgdprs151010429
ensemblrs151010429
gopubmedrs151010429
geneviewrs151010429
scholarrs151010429
googlers151010429
pharmgkbrs151010429
gwascentralrs151010429
openSNPrs151010429
23andMers151010429
23andMe allrs151010429
SNP Nexus

SNPshotrs151010429
SNPdbers151010429
MSV3drs151010429
GWAS Ctlgrs151010429
Max Magnitude0
ClinVar
Risk rs151010429(A,T;A,T)
Alt rs151010429(A,T;A,T)
Reference rs151010429(G;G)
Significance Other
Disease Arrhythmogenic right ventricular cardiomyopathy not provided
Variation info
Gene TMEM43
CLNDBN Arrhythmogenic right ventricular cardiomyopathy, type 5 not provided
Reversed 0
HGVS NC_000003.11:g.14172328G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000074479.4, RCV000172115.1,