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rs770029258

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs770029258(C;C)
Make rs770029258(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178759167
GeneTTN
is asnp
is mentioned by
dbSNPrs770029258
ebirs770029258
HLIrs770029258
Exacrs770029258
Varsomers770029258
Maprs770029258
PheGenIrs770029258
hapmaprs770029258
1000 genomesrs770029258
hgdprs770029258
ensemblrs770029258
gopubmedrs770029258
geneviewrs770029258
scholarrs770029258
googlers770029258
pharmgkbrs770029258
gwascentralrs770029258
openSNPrs770029258
23andMers770029258
23andMe allrs770029258
SNP Nexus

SNPshotrs770029258
SNPdbers770029258
MSV3drs770029258
GWAS Ctlgrs770029258
Max Magnitude0
ClinVar
Risk rs770029258(A,C;A,C)
Alt rs770029258(A,C;A,C)
Reference rs770029258(T;T)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN
CLNDBN Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000002.11:g.179623894T>A
CLNSRC
CLNACC RCV000208494.1,