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rs727504243

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727504243(C;T)
Make rs727504243(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position55151857
GeneTNNI3
is asnp
is mentioned by
dbSNPrs727504243
ebirs727504243
HLIrs727504243
Exacrs727504243
Varsomers727504243
Maprs727504243
PheGenIrs727504243
hapmaprs727504243
1000 genomesrs727504243
hgdprs727504243
ensemblrs727504243
gopubmedrs727504243
geneviewrs727504243
scholarrs727504243
googlers727504243
pharmgkbrs727504243
gwascentralrs727504243
openSNPrs727504243
23andMers727504243
23andMe allrs727504243
SNP Nexus

SNPshotrs727504243
SNPdbers727504243
MSV3drs727504243
GWAS Ctlgrs727504243
Max Magnitude0
ClinVar
Risk rs727504243(T;T)
Alt rs727504243(T;T)
Reference rs727504243(C;C)
Significance Pathogenic
Disease not specified not provided Familial hypertrophic cardiomyopathy 7
Variation info
Gene TNNI3
CLNDBN not specified not provided Familial hypertrophic cardiomyopathy 7
Reversed 1
HGVS NC_000019.9:g.55663225G>A
CLNSRC
CLNACC RCV000154213.2, RCV000159248.2, RCV000168956.1,