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rs869312115

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312115(A;A)
Make rs869312115(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178573023
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs869312115
ebirs869312115
HLIrs869312115
Exacrs869312115
Varsomers869312115
Maprs869312115
PheGenIrs869312115
hapmaprs869312115
1000 genomesrs869312115
hgdprs869312115
ensemblrs869312115
gopubmedrs869312115
geneviewrs869312115
scholarrs869312115
googlers869312115
pharmgkbrs869312115
gwascentralrs869312115
openSNPrs869312115
23andMers869312115
23andMe allrs869312115
SNP Nexus

SNPshotrs869312115
SNPdbers869312115
MSV3drs869312115
GWAS Ctlgrs869312115
Max Magnitude0
ClinVar
Risk rs869312115(A;A)
Alt rs869312115(A;A)
Reference rs869312115(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.179437750C>T
CLNSRC
CLNACC RCV000209791.1,