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rs869312068

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312068(A;A)
Make rs869312068(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178534619
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs869312068
ebirs869312068
HLIrs869312068
Exacrs869312068
Varsomers869312068
Maprs869312068
PheGenIrs869312068
hapmaprs869312068
1000 genomesrs869312068
hgdprs869312068
ensemblrs869312068
gopubmedrs869312068
geneviewrs869312068
scholarrs869312068
googlers869312068
pharmgkbrs869312068
gwascentralrs869312068
openSNPrs869312068
23andMers869312068
23andMe allrs869312068
SNP Nexus

SNPshotrs869312068
SNPdbers869312068
MSV3drs869312068
GWAS Ctlgrs869312068
Max Magnitude0
ClinVar
Risk rs869312068(A;A)
Alt rs869312068(A;A)
Reference rs869312068(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.179399346C>T
CLNSRC
CLNACC RCV000208945.1,