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rs876657669

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876657669(-;-)
Make rs876657669(-;A)
Make rs876657669(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178573299
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs876657669
ebirs876657669
HLIrs876657669
Exacrs876657669
Varsomers876657669
Maprs876657669
PheGenIrs876657669
hapmaprs876657669
1000 genomesrs876657669
hgdprs876657669
ensemblrs876657669
gopubmedrs876657669
geneviewrs876657669
scholarrs876657669
googlers876657669
pharmgkbrs876657669
gwascentralrs876657669
openSNPrs876657669
23andMers876657669
23andMe allrs876657669
SNP Nexus

SNPshotrs876657669
SNPdbers876657669
MSV3drs876657669
GWAS Ctlgrs876657669
Max Magnitude0
ClinVar
Risk rs876657669(A;A)
Alt rs876657669(A;A)
Reference rs876657669(;)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179438027dupT
CLNSRC
CLNACC RCV000216886.1,