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rs876657663

From SNPedia

Orientationminus
Geno Mag Summary
(ACACGTT;ACACGTT) 0 common in clinvar
Make rs876657663(-;-)
Make rs876657663(-;ACACGTT)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178759040
GeneTTN
is asnp
is mentioned by
dbSNPrs876657663
ebirs876657663
HLIrs876657663
Exacrs876657663
Varsomers876657663
Maprs876657663
PheGenIrs876657663
hapmaprs876657663
1000 genomesrs876657663
hgdprs876657663
ensemblrs876657663
gopubmedrs876657663
geneviewrs876657663
scholarrs876657663
googlers876657663
pharmgkbrs876657663
gwascentralrs876657663
openSNPrs876657663
23andMers876657663
23andMe allrs876657663
SNP Nexus

SNPshotrs876657663
SNPdbers876657663
MSV3drs876657663
GWAS Ctlgrs876657663
Max Magnitude0
ClinVar
Risk rs876657663(;)
Alt rs876657663(;)
Reference rs876657663(ACACGTT;ACACGTT)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179623767_179623773delAACGTGT
CLNSRC
CLNACC RCV000214597.1,