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rs727503503

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727503503(A;A)
Make rs727503503(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position55154070
GeneTNNI3
is asnp
is mentioned by
dbSNPrs727503503
ebirs727503503
HLIrs727503503
Exacrs727503503
Varsomers727503503
Maprs727503503
PheGenIrs727503503
hapmaprs727503503
1000 genomesrs727503503
hgdprs727503503
ensemblrs727503503
gopubmedrs727503503
geneviewrs727503503
scholarrs727503503
googlers727503503
pharmgkbrs727503503
gwascentralrs727503503
openSNPrs727503503
23andMers727503503
23andMe allrs727503503
SNP Nexus

SNPshotrs727503503
SNPdbers727503503
MSV3drs727503503
GWAS Ctlgrs727503503
Max Magnitude0
ClinVar
Risk rs727503503(A;A)
Alt rs727503503(A;A)
Reference rs727503503(G;G)
Significance Other
Disease Cardiomyopathy not provided
Variation info
Gene TNNI3
CLNDBN Cardiomyopathy not provided
Reversed 1
HGVS NC_000019.9:g.55665438C>T
CLNSRC
CLNACC RCV000152076.2, RCV000159232.2,