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rs869312060

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs869312060(-;-)
Make rs869312060(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178563619
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs869312060
ebirs869312060
HLIrs869312060
Exacrs869312060
Varsomers869312060
Maprs869312060
PheGenIrs869312060
hapmaprs869312060
1000 genomesrs869312060
hgdprs869312060
ensemblrs869312060
gopubmedrs869312060
geneviewrs869312060
scholarrs869312060
googlers869312060
pharmgkbrs869312060
gwascentralrs869312060
openSNPrs869312060
23andMers869312060
23andMe allrs869312060
SNP Nexus

SNPshotrs869312060
SNPdbers869312060
MSV3drs869312060
GWAS Ctlgrs869312060
Max Magnitude0
ClinVar
Risk rs869312060(;)
Alt rs869312060(;)
Reference rs869312060(A;A)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179428346delT
CLNSRC
CLNACC RCV000209053.1,