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rs751039219

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs751039219(A;A)
Make rs751039219(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178532605
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs751039219
ebirs751039219
HLIrs751039219
Exacrs751039219
Varsomers751039219
Maprs751039219
PheGenIrs751039219
hapmaprs751039219
1000 genomesrs751039219
hgdprs751039219
ensemblrs751039219
gopubmedrs751039219
geneviewrs751039219
scholarrs751039219
googlers751039219
pharmgkbrs751039219
gwascentralrs751039219
openSNPrs751039219
23andMers751039219
23andMe allrs751039219
SNP Nexus

SNPshotrs751039219
SNPdbers751039219
MSV3drs751039219
GWAS Ctlgrs751039219
Max Magnitude0
ClinVar
Risk rs751039219(A;A)
Alt rs751039219(A;A)
Reference rs751039219(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.179397332G>T
CLNSRC
CLNACC RCV000208249.1,