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rs869312077

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs869312077(-;-)
Make rs869312077(-;A)
Make rs869312077(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178570015
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs869312077
ebirs869312077
HLIrs869312077
Exacrs869312077
Varsomers869312077
Maprs869312077
PheGenIrs869312077
hapmaprs869312077
1000 genomesrs869312077
hgdprs869312077
ensemblrs869312077
gopubmedrs869312077
geneviewrs869312077
scholarrs869312077
googlers869312077
pharmgkbrs869312077
gwascentralrs869312077
openSNPrs869312077
23andMers869312077
23andMe allrs869312077
SNP Nexus

SNPshotrs869312077
SNPdbers869312077
MSV3drs869312077
GWAS Ctlgrs869312077
Max Magnitude0
ClinVar
Risk rs869312077(A;A)
Alt rs869312077(A;A)
Reference rs869312077(;)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179434742_179434743insT
CLNSRC
CLNACC RCV000209355.1,