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rs727503506

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727503506(C;C)
Make rs727503506(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position55154743
GeneTNNI3
is asnp
is mentioned by
dbSNPrs727503506
ebirs727503506
HLIrs727503506
Exacrs727503506
Varsomers727503506
Maprs727503506
PheGenIrs727503506
hapmaprs727503506
1000 genomesrs727503506
hgdprs727503506
ensemblrs727503506
gopubmedrs727503506
geneviewrs727503506
scholarrs727503506
googlers727503506
pharmgkbrs727503506
gwascentralrs727503506
openSNPrs727503506
23andMers727503506
23andMe allrs727503506
SNP Nexus

SNPshotrs727503506
SNPdbers727503506
MSV3drs727503506
GWAS Ctlgrs727503506
Max Magnitude0
ClinVar
Risk rs727503506(C;C)
Alt rs727503506(C;C)
Reference rs727503506(G;G)
Significance Probable-Pathogenic
Disease not specified Hypertrophic cardiomyopathy
Variation info
Gene TNNI3
CLNDBN not specified Hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000019.9:g.55666111C>G
CLNSRC
CLNACC RCV000152086.3, RCV000233460.1,