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rs869312047

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312047(A;A)
Make rs869312047(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178617119
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs869312047
ebirs869312047
HLIrs869312047
Exacrs869312047
Varsomers869312047
Maprs869312047
PheGenIrs869312047
hapmaprs869312047
1000 genomesrs869312047
hgdprs869312047
ensemblrs869312047
gopubmedrs869312047
geneviewrs869312047
scholarrs869312047
googlers869312047
pharmgkbrs869312047
gwascentralrs869312047
openSNPrs869312047
23andMers869312047
23andMe allrs869312047
SNP Nexus

SNPshotrs869312047
SNPdbers869312047
MSV3drs869312047
GWAS Ctlgrs869312047
Max Magnitude0
ClinVar
Risk rs869312047(A;A)
Alt rs869312047(A;A)
Reference rs869312047(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.179481846C>T
CLNSRC
CLNACC RCV000209417.1,