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rs730880231

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880231(C;C)
Make rs730880231(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position55154057
GeneTNNI3
is asnp
is mentioned by
dbSNPrs730880231
ebirs730880231
HLIrs730880231
Exacrs730880231
Varsomers730880231
Maprs730880231
PheGenIrs730880231
hapmaprs730880231
1000 genomesrs730880231
hgdprs730880231
ensemblrs730880231
gopubmedrs730880231
geneviewrs730880231
scholarrs730880231
googlers730880231
pharmgkbrs730880231
gwascentralrs730880231
openSNPrs730880231
23andMers730880231
23andMe allrs730880231
SNP Nexus

SNPshotrs730880231
SNPdbers730880231
MSV3drs730880231
GWAS Ctlgrs730880231
Max Magnitude0
ClinVar
Risk rs730880231(C;C)
Alt rs730880231(C;C)
Reference rs730880231(G;G)
Significance Pathogenic
Disease Cardiomyopathy
Variation info
Gene TNNI3
CLNDBN Cardiomyopathy, restrictive
Reversed 1
HGVS NC_000019.9:g.55665425C>G
CLNSRC
CLNACC RCV000157531.1,