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rs869312061

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869312061(-;-)
Make rs869312061(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178559491
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs869312061
ebirs869312061
HLIrs869312061
Exacrs869312061
Varsomers869312061
Maprs869312061
PheGenIrs869312061
hapmaprs869312061
1000 genomesrs869312061
hgdprs869312061
ensemblrs869312061
gopubmedrs869312061
geneviewrs869312061
scholarrs869312061
googlers869312061
pharmgkbrs869312061
gwascentralrs869312061
openSNPrs869312061
23andMers869312061
23andMe allrs869312061
SNP Nexus

SNPshotrs869312061
SNPdbers869312061
MSV3drs869312061
GWAS Ctlgrs869312061
Max Magnitude0
ClinVar
Risk rs869312061(;)
Alt rs869312061(;)
Reference rs869312061(C;C)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179424218delG
CLNSRC
CLNACC RCV000209817.1,