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rs727503501

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727503501(A;A)
Make rs727503501(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position55154053
GeneTNNI3
is asnp
is mentioned by
dbSNPrs727503501
ebirs727503501
HLIrs727503501
Exacrs727503501
Varsomers727503501
Maprs727503501
PheGenIrs727503501
hapmaprs727503501
1000 genomesrs727503501
hgdprs727503501
ensemblrs727503501
gopubmedrs727503501
geneviewrs727503501
scholarrs727503501
googlers727503501
pharmgkbrs727503501
gwascentralrs727503501
openSNPrs727503501
23andMers727503501
23andMe allrs727503501
SNP Nexus

SNPshotrs727503501
SNPdbers727503501
MSV3drs727503501
GWAS Ctlgrs727503501
Max Magnitude0
ClinVar
Risk rs727503501(A;A)
Alt rs727503501(A;A)
Reference rs727503501(G;G)
Significance Probable-Pathogenic
Disease not specified Primary familial hypertrophic cardiomyopathy
Variation info
Gene TNNI3
CLNDBN not specified Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000019.9:g.55665421C>T
CLNSRC
CLNACC RCV000152074.1, RCV000157532.1,