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rs730881069

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730881069(A;A)
Make rs730881069(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position55154172
GeneTNNI3
is asnp
is mentioned by
dbSNPrs730881069
ebirs730881069
HLIrs730881069
Exacrs730881069
Varsomers730881069
Maprs730881069
PheGenIrs730881069
hapmaprs730881069
1000 genomesrs730881069
hgdprs730881069
ensemblrs730881069
gopubmedrs730881069
geneviewrs730881069
scholarrs730881069
googlers730881069
pharmgkbrs730881069
gwascentralrs730881069
openSNPrs730881069
23andMers730881069
23andMe allrs730881069
SNP Nexus

SNPshotrs730881069
SNPdbers730881069
MSV3drs730881069
GWAS Ctlgrs730881069
Max Magnitude0
ClinVar
Risk rs730881069(A;A)
Alt rs730881069(A;A)
Reference rs730881069(G;G)
Significance Pathogenic
Disease not provided Hypertrophic cardiomyopathy
Variation info
Gene TNNI3
CLNDBN not provided Hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000019.9:g.55665540C>T
CLNSRC
CLNACC RCV000159213.2, RCV000167999.1,