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rs876657668

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876657668(C;C)
Make rs876657668(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178585348
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs876657668
ebirs876657668
HLIrs876657668
Exacrs876657668
Varsomers876657668
Maprs876657668
PheGenIrs876657668
hapmaprs876657668
1000 genomesrs876657668
hgdprs876657668
ensemblrs876657668
gopubmedrs876657668
geneviewrs876657668
scholarrs876657668
googlers876657668
pharmgkbrs876657668
gwascentralrs876657668
openSNPrs876657668
23andMers876657668
23andMe allrs876657668
SNP Nexus

SNPshotrs876657668
SNPdbers876657668
MSV3drs876657668
GWAS Ctlgrs876657668
Max Magnitude0
ClinVar
Risk rs876657668(C;C)
Alt rs876657668(C;C)
Reference rs876657668(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.179450075C>G
CLNSRC
CLNACC RCV000222488.1,