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rs876657670

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876657670(G;T)
Make rs876657670(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178560622
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs876657670
ebirs876657670
HLIrs876657670
Exacrs876657670
Varsomers876657670
Maprs876657670
PheGenIrs876657670
hapmaprs876657670
1000 genomesrs876657670
hgdprs876657670
ensemblrs876657670
gopubmedrs876657670
geneviewrs876657670
scholarrs876657670
googlers876657670
pharmgkbrs876657670
gwascentralrs876657670
openSNPrs876657670
23andMers876657670
23andMe allrs876657670
SNP Nexus

SNPshotrs876657670
SNPdbers876657670
MSV3drs876657670
GWAS Ctlgrs876657670
Max Magnitude0
ClinVar
Risk rs876657670(T;T)
Alt rs876657670(T;T)
Reference rs876657670(G;G)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179425349C>A
CLNSRC
CLNACC RCV000213508.1,