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rs876657673

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876657673(-;-)
Make rs876657673(-;T)
Make rs876657673(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178739618
GeneTTN
is asnp
is mentioned by
dbSNPrs876657673
ebirs876657673
HLIrs876657673
Exacrs876657673
Varsomers876657673
Maprs876657673
PheGenIrs876657673
hapmaprs876657673
1000 genomesrs876657673
hgdprs876657673
ensemblrs876657673
gopubmedrs876657673
geneviewrs876657673
scholarrs876657673
googlers876657673
pharmgkbrs876657673
gwascentralrs876657673
openSNPrs876657673
23andMers876657673
23andMe allrs876657673
SNP Nexus

SNPshotrs876657673
SNPdbers876657673
MSV3drs876657673
GWAS Ctlgrs876657673
Max Magnitude0
ClinVar
Risk rs876657673(T;T)
Alt rs876657673(T;T)
Reference rs876657673(;)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179604346dupA
CLNSRC
CLNACC RCV000214051.1,