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rs727503586

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs727503586(A;A)
Make rs727503586(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position178589508
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs727503586
ebirs727503586
HLIrs727503586
Exacrs727503586
Varsomers727503586
Maprs727503586
PheGenIrs727503586
hapmaprs727503586
1000 genomesrs727503586
hgdprs727503586
ensemblrs727503586
gopubmedrs727503586
geneviewrs727503586
scholarrs727503586
googlers727503586
pharmgkbrs727503586
gwascentralrs727503586
openSNPrs727503586
23andMers727503586
23andMe allrs727503586
SNP Nexus

SNPshotrs727503586
SNPdbers727503586
MSV3drs727503586
GWAS Ctlgrs727503586
Max Magnitude0
ClinVar
Risk rs727503586(A;A)
Alt rs727503586(A;A)
Reference rs727503586(T;T)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179454235A>T
CLNSRC
CLNACC RCV000152265.1,