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rs368861241

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs368861241(A;A)
Make rs368861241(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position55154095
GeneTNNI3
is asnp
is mentioned by
dbSNPrs368861241
ebirs368861241
HLIrs368861241
Exacrs368861241
Varsomers368861241
Maprs368861241
PheGenIrs368861241
hapmaprs368861241
1000 genomesrs368861241
hgdprs368861241
ensemblrs368861241
gopubmedrs368861241
geneviewrs368861241
scholarrs368861241
googlers368861241
pharmgkbrs368861241
gwascentralrs368861241
openSNPrs368861241
23andMers368861241
23andMe allrs368861241
SNP Nexus

SNPshotrs368861241
SNPdbers368861241
MSV3drs368861241
GWAS Ctlgrs368861241
Max Magnitude0
ClinVar
Risk rs368861241(A;A)
Alt rs368861241(A;A)
Reference rs368861241(G;G)
Significance Pathogenic
Disease Primary familial hypertrophic cardiomyopathy not specified not provided Familial hypertrophic cardiomyopathy 7
Variation info
Gene TNNI3
CLNDBN Primary familial hypertrophic cardiomyopathy not specified not provided Familial hypertrophic cardiomyopathy 7
Reversed 0
HGVS NC_000019.9:g.55665463G>A
CLNSRC
CLNACC RCV000148896.1, RCV000154211.1, RCV000159228.2, RCV000168952.1,