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rs876657667

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876657667(A;G)
Make rs876657667(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178586809
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs876657667
ebirs876657667
HLIrs876657667
Exacrs876657667
Varsomers876657667
Maprs876657667
PheGenIrs876657667
hapmaprs876657667
1000 genomesrs876657667
hgdprs876657667
ensemblrs876657667
gopubmedrs876657667
geneviewrs876657667
scholarrs876657667
googlers876657667
pharmgkbrs876657667
gwascentralrs876657667
openSNPrs876657667
23andMers876657667
23andMe allrs876657667
SNP Nexus

SNPshotrs876657667
SNPdbers876657667
MSV3drs876657667
GWAS Ctlgrs876657667
Max Magnitude0
ClinVar
Risk rs876657667(G;G)
Alt rs876657667(G;G)
Reference rs876657667(A;A)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179451536T>C
CLNSRC
CLNACC RCV000218778.1,