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rs727503658

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs727503658(-;-)
Make rs727503658(-;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position178740828
GeneTTN
is asnp
is mentioned by
dbSNPrs727503658
ebirs727503658
HLIrs727503658
Exacrs727503658
Varsomers727503658
Maprs727503658
PheGenIrs727503658
hapmaprs727503658
1000 genomesrs727503658
hgdprs727503658
ensemblrs727503658
gopubmedrs727503658
geneviewrs727503658
scholarrs727503658
googlers727503658
pharmgkbrs727503658
gwascentralrs727503658
openSNPrs727503658
23andMers727503658
23andMe allrs727503658
SNP Nexus

SNPshotrs727503658
SNPdbers727503658
MSV3drs727503658
GWAS Ctlgrs727503658
Max Magnitude0
ClinVar
Risk rs727503658(;)
Alt rs727503658(;)
Reference rs727503658(T;T)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy not provided
Variation info
Gene TTN
CLNDBN Primary dilated cardiomyopathy not provided
Reversed 1
HGVS NC_000002.11:g.179605555delA
CLNSRC
CLNACC RCV000152420.1, RCV000184415.1,