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rs727504365

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs727504365(C;C)
Make rs727504365(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position55151865
GeneTNNI3
is asnp
is mentioned by
dbSNPrs727504365
ebirs727504365
HLIrs727504365
Exacrs727504365
Varsomers727504365
Maprs727504365
PheGenIrs727504365
hapmaprs727504365
1000 genomesrs727504365
hgdprs727504365
ensemblrs727504365
gopubmedrs727504365
geneviewrs727504365
scholarrs727504365
googlers727504365
pharmgkbrs727504365
gwascentralrs727504365
openSNPrs727504365
23andMers727504365
23andMe allrs727504365
SNP Nexus

SNPshotrs727504365
SNPdbers727504365
MSV3drs727504365
GWAS Ctlgrs727504365
Max Magnitude0
ClinVar
Risk rs727504365(C;C)
Alt rs727504365(C;C)
Reference rs727504365(T;T)
Significance Probable-Pathogenic
Disease Primary familial hypertrophic cardiomyopathy
Variation info
Gene TNNI3
CLNDBN Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000019.9:g.55663233A>G
CLNSRC
CLNACC RCV000154501.2,