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rs730881091

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730881091(A;A)
Make rs730881091(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position55151871
GeneTNNI3
is asnp
is mentioned by
dbSNPrs730881091
ebirs730881091
HLIrs730881091
Exacrs730881091
Varsomers730881091
Maprs730881091
PheGenIrs730881091
hapmaprs730881091
1000 genomesrs730881091
hgdprs730881091
ensemblrs730881091
gopubmedrs730881091
geneviewrs730881091
scholarrs730881091
googlers730881091
pharmgkbrs730881091
gwascentralrs730881091
openSNPrs730881091
23andMers730881091
23andMe allrs730881091
SNP Nexus

SNPshotrs730881091
SNPdbers730881091
MSV3drs730881091
GWAS Ctlgrs730881091
Max Magnitude0
ClinVar
Risk rs730881091(A;A)
Alt rs730881091(A;A)
Reference rs730881091(G;G)
Significance Probable-Pathogenic
Disease not specified Familial hypertrophic cardiomyopathy 7 not provided
Variation info
Gene TNNI3
CLNDBN not specified Familial hypertrophic cardiomyopathy 7 not provided
Reversed 1
HGVS NC_000019.9:g.55663239C>T
CLNSRC
CLNACC RCV000168955.1, RCV000201449.1, RCV000225742.1,