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rs876657666

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876657666(-;-)
Make rs876657666(-;C)
Make rs876657666(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178588815
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs876657666
ebirs876657666
HLIrs876657666
Exacrs876657666
Varsomers876657666
Maprs876657666
PheGenIrs876657666
hapmaprs876657666
1000 genomesrs876657666
hgdprs876657666
ensemblrs876657666
gopubmedrs876657666
geneviewrs876657666
scholarrs876657666
googlers876657666
pharmgkbrs876657666
gwascentralrs876657666
openSNPrs876657666
23andMers876657666
23andMe allrs876657666
SNP Nexus

SNPshotrs876657666
SNPdbers876657666
MSV3drs876657666
GWAS Ctlgrs876657666
Max Magnitude0
ClinVar
Risk rs876657666(C;C)
Alt rs876657666(C;C)
Reference rs876657666(;)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179453543dupG
CLNSRC
CLNACC RCV000216412.1,