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rs876657664

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876657664(-;-)
Make rs876657664(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178636088
GeneTTN
is asnp
is mentioned by
dbSNPrs876657664
ebirs876657664
HLIrs876657664
Exacrs876657664
Varsomers876657664
Maprs876657664
PheGenIrs876657664
hapmaprs876657664
1000 genomesrs876657664
hgdprs876657664
ensemblrs876657664
gopubmedrs876657664
geneviewrs876657664
scholarrs876657664
googlers876657664
pharmgkbrs876657664
gwascentralrs876657664
openSNPrs876657664
23andMers876657664
23andMe allrs876657664
SNP Nexus

SNPshotrs876657664
SNPdbers876657664
MSV3drs876657664
GWAS Ctlgrs876657664
Max Magnitude0
ClinVar
Risk rs876657664(;)
Alt rs876657664(;)
Reference rs876657664(C;C)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179500815delG
CLNSRC
CLNACC RCV000219662.1,