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rs146336815

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs146336815(A;G)
Make rs146336815(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position68122283
GeneMYPN
is asnp
is mentioned by
dbSNPrs146336815
ebirs146336815
HLIrs146336815
Exacrs146336815
Varsomers146336815
Maprs146336815
PheGenIrs146336815
hapmaprs146336815
1000 genomesrs146336815
hgdprs146336815
ensemblrs146336815
gopubmedrs146336815
geneviewrs146336815
scholarrs146336815
googlers146336815
pharmgkbrs146336815
gwascentralrs146336815
openSNPrs146336815
23andMers146336815
23andMe allrs146336815
SNP Nexus

SNPshotrs146336815
SNPdbers146336815
MSV3drs146336815
GWAS Ctlgrs146336815
Max Magnitude0
ClinVar
Risk rs146336815(G;G)
Alt rs146336815(G;G)
Reference rs146336815(A;A)
Significance Probable-Pathogenic
Disease Cardiomyopathy
Variation info
Gene MYPN
CLNDBN Cardiomyopathy
Reversed 0
HGVS NC_000010.10:g.69882040A>G
CLNSRC
CLNACC RCV000183580.1,