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rs768345594

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs768345594(G;T)
Make rs768345594(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178585291
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs768345594
ebirs768345594
HLIrs768345594
Exacrs768345594
Varsomers768345594
Maprs768345594
PheGenIrs768345594
hapmaprs768345594
1000 genomesrs768345594
hgdprs768345594
ensemblrs768345594
gopubmedrs768345594
geneviewrs768345594
scholarrs768345594
googlers768345594
pharmgkbrs768345594
gwascentralrs768345594
openSNPrs768345594
23andMers768345594
23andMe allrs768345594
SNP Nexus

SNPshotrs768345594
SNPdbers768345594
MSV3drs768345594
GWAS Ctlgrs768345594
Max Magnitude0
ClinVar
Risk rs768345594(A,T;A,T)
Alt rs768345594(A,T;A,T)
Reference rs768345594(G;G)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000002.11:g.179450018G>A
CLNSRC
CLNACC RCV000209173.1,