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rs876657665

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876657665(C;C)
Make rs876657665(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178614754
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs876657665
ebirs876657665
HLIrs876657665
Exacrs876657665
Varsomers876657665
Maprs876657665
PheGenIrs876657665
hapmaprs876657665
1000 genomesrs876657665
hgdprs876657665
ensemblrs876657665
gopubmedrs876657665
geneviewrs876657665
scholarrs876657665
googlers876657665
pharmgkbrs876657665
gwascentralrs876657665
openSNPrs876657665
23andMers876657665
23andMe allrs876657665
SNP Nexus

SNPshotrs876657665
SNPdbers876657665
MSV3drs876657665
GWAS Ctlgrs876657665
Max Magnitude0
ClinVar
Risk rs876657665(C;C)
Alt rs876657665(C;C)
Reference rs876657665(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.179479481C>G
CLNSRC
CLNACC RCV000215023.1,