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rs869312056

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs869312056(-;-)
Make rs869312056(-;A)
Make rs869312056(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178571825
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs869312056
ebirs869312056
HLIrs869312056
Exacrs869312056
Varsomers869312056
Maprs869312056
PheGenIrs869312056
hapmaprs869312056
1000 genomesrs869312056
hgdprs869312056
ensemblrs869312056
gopubmedrs869312056
geneviewrs869312056
scholarrs869312056
googlers869312056
pharmgkbrs869312056
gwascentralrs869312056
openSNPrs869312056
23andMers869312056
23andMe allrs869312056
SNP Nexus

SNPshotrs869312056
SNPdbers869312056
MSV3drs869312056
GWAS Ctlgrs869312056
Max Magnitude0
ClinVar
Risk rs869312056(A;A)
Alt rs869312056(A;A)
Reference rs869312056(;)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179436553dupT
CLNSRC
CLNACC RCV000209326.1,