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rs779996703

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs779996703(G;T)
Make rs779996703(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178567141
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs779996703
ebirs779996703
HLIrs779996703
Exacrs779996703
Varsomers779996703
Maprs779996703
PheGenIrs779996703
hapmaprs779996703
1000 genomesrs779996703
hgdprs779996703
ensemblrs779996703
gopubmedrs779996703
geneviewrs779996703
scholarrs779996703
googlers779996703
pharmgkbrs779996703
gwascentralrs779996703
openSNPrs779996703
23andMers779996703
23andMe allrs779996703
SNP Nexus

SNPshotrs779996703
SNPdbers779996703
MSV3drs779996703
GWAS Ctlgrs779996703
Max Magnitude0
ClinVar
Risk rs779996703(T;T)
Alt rs779996703(T;T)
Reference rs779996703(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.179431868G>A
CLNSRC
CLNACC RCV000209202.1,