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rs868494032

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs868494032(A;A)
Make rs868494032(A;C)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178559695
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs868494032
ebirs868494032
HLIrs868494032
Exacrs868494032
Varsomers868494032
Maprs868494032
PheGenIrs868494032
hapmaprs868494032
1000 genomesrs868494032
hgdprs868494032
ensemblrs868494032
gopubmedrs868494032
geneviewrs868494032
scholarrs868494032
googlers868494032
pharmgkbrs868494032
gwascentralrs868494032
openSNPrs868494032
23andMers868494032
23andMe allrs868494032
SNP Nexus

SNPshotrs868494032
SNPdbers868494032
MSV3drs868494032
GWAS Ctlgrs868494032
Max Magnitude0
ClinVar
Risk rs868494032(A,T;A,T)
Alt rs868494032(A,T;A,T)
Reference rs868494032(C;C)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000002.11:g.179424422C>A
CLNSRC
CLNACC RCV000216926.1,