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rs727504872

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727504872(-;-)
Make rs727504872(-;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position55156279
GeneTNNI3
is asnp
is mentioned by
dbSNPrs727504872
ebirs727504872
HLIrs727504872
Exacrs727504872
Varsomers727504872
Maprs727504872
PheGenIrs727504872
hapmaprs727504872
1000 genomesrs727504872
hgdprs727504872
ensemblrs727504872
gopubmedrs727504872
geneviewrs727504872
scholarrs727504872
googlers727504872
pharmgkbrs727504872
gwascentralrs727504872
openSNPrs727504872
23andMers727504872
23andMe allrs727504872
SNP Nexus

SNPshotrs727504872
SNPdbers727504872
MSV3drs727504872
GWAS Ctlgrs727504872
Max Magnitude0
ClinVar
Risk rs727504872(;)
Alt rs727504872(;)
Reference rs727504872(G;G)
Significance Probable-Pathogenic
Disease Cardiomyopathy not specified not provided
Variation info
Gene TNNI3
CLNDBN Cardiomyopathy not specified not provided
Reversed 1
HGVS NC_000019.9:g.55667647delC
CLNSRC
CLNACC RCV000156236.1, RCV000159255.2, RCV000223861.1,