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rs876657672

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876657672(A;A)
Make rs876657672(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178537244
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs876657672
ebirs876657672
HLIrs876657672
Exacrs876657672
Varsomers876657672
Maprs876657672
PheGenIrs876657672
hapmaprs876657672
1000 genomesrs876657672
hgdprs876657672
ensemblrs876657672
gopubmedrs876657672
geneviewrs876657672
scholarrs876657672
googlers876657672
pharmgkbrs876657672
gwascentralrs876657672
openSNPrs876657672
23andMers876657672
23andMe allrs876657672
SNP Nexus

SNPshotrs876657672
SNPdbers876657672
MSV3drs876657672
GWAS Ctlgrs876657672
Max Magnitude0
ClinVar
Risk rs876657672(A;A)
Alt rs876657672(A;A)
Reference rs876657672(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.179401971C>T
CLNSRC
CLNACC RCV000222308.1,