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rs876657671

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876657671(C;T)
Make rs876657671(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178543876
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs876657671
ebirs876657671
HLIrs876657671
Exacrs876657671
Varsomers876657671
Maprs876657671
PheGenIrs876657671
hapmaprs876657671
1000 genomesrs876657671
hgdprs876657671
ensemblrs876657671
gopubmedrs876657671
geneviewrs876657671
scholarrs876657671
googlers876657671
pharmgkbrs876657671
gwascentralrs876657671
openSNPrs876657671
23andMers876657671
23andMe allrs876657671
SNP Nexus

SNPshotrs876657671
SNPdbers876657671
MSV3drs876657671
GWAS Ctlgrs876657671
Max Magnitude0
ClinVar
Risk rs876657671(T;T)
Alt rs876657671(T;T)
Reference rs876657671(C;C)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179408603G>A
CLNSRC
CLNACC RCV000213569.1,