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rs151282801

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151282801(C;T)
Make rs151282801(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position68195498
GeneMYPN
is asnp
is mentioned by
dbSNPrs151282801
ebirs151282801
HLIrs151282801
Exacrs151282801
Varsomers151282801
Maprs151282801
PheGenIrs151282801
hapmaprs151282801
1000 genomesrs151282801
hgdprs151282801
ensemblrs151282801
gopubmedrs151282801
geneviewrs151282801
scholarrs151282801
googlers151282801
pharmgkbrs151282801
gwascentralrs151282801
openSNPrs151282801
23andMers151282801
23andMe allrs151282801
SNP Nexus

SNPshotrs151282801
SNPdbers151282801
MSV3drs151282801
GWAS Ctlgrs151282801
Max Magnitude0
ClinVar
Risk rs151282801(T;T)
Alt rs151282801(T;T)
Reference rs151282801(C;C)
Significance Probable-non-pathogenic
Disease Primary familial hypertrophic cardiomyopathy Dilated cardiomyopathy 1KK
Variation info
Gene MYPN
CLNDBN Primary familial hypertrophic cardiomyopathy Dilated cardiomyopathy 1KK
Reversed 0
HGVS NC_000010.10:g.69955255C>T
CLNSRC ClinVar
CLNACC RCV000143934.2, RCV000228976.1,