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rs587782987

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587782987(C;T)
Make rs587782987(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position178611274
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs587782987
ebirs587782987
HLIrs587782987
Exacrs587782987
Varsomers587782987
Maprs587782987
PheGenIrs587782987
hapmaprs587782987
1000 genomesrs587782987
hgdprs587782987
ensemblrs587782987
gopubmedrs587782987
geneviewrs587782987
scholarrs587782987
googlers587782987
pharmgkbrs587782987
gwascentralrs587782987
openSNPrs587782987
23andMers587782987
23andMe allrs587782987
SNP Nexus

SNPshotrs587782987
SNPdbers587782987
MSV3drs587782987
GWAS Ctlgrs587782987
Max Magnitude0
ClinVar
Risk rs587782987(T;T)
Alt rs587782987(T;T)
Reference rs587782987(C;C)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy not specified
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy not specified
Reversed 1
HGVS NC_000002.11:g.179476001G>A
CLNSRC
CLNACC RCV000143972.2, RCV000225702.1,