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rs869312073

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312073(A;A)
Make rs869312073(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178592278
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs869312073
ebirs869312073
HLIrs869312073
Exacrs869312073
Varsomers869312073
Maprs869312073
PheGenIrs869312073
hapmaprs869312073
1000 genomesrs869312073
hgdprs869312073
ensemblrs869312073
gopubmedrs869312073
geneviewrs869312073
scholarrs869312073
googlers869312073
pharmgkbrs869312073
gwascentralrs869312073
openSNPrs869312073
23andMers869312073
23andMe allrs869312073
SNP Nexus

SNPshotrs869312073
SNPdbers869312073
MSV3drs869312073
GWAS Ctlgrs869312073
Max Magnitude0
ClinVar
Risk rs869312073(A;A)
Alt rs869312073(A;A)
Reference rs869312073(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.179457005C>T
CLNSRC
CLNACC RCV000209368.1,