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rs727505352

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727505352(A;A)
Make rs727505352(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position178578835
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs727505352
ebirs727505352
HLIrs727505352
Exacrs727505352
Varsomers727505352
Maprs727505352
PheGenIrs727505352
hapmaprs727505352
1000 genomesrs727505352
hgdprs727505352
ensemblrs727505352
gopubmedrs727505352
geneviewrs727505352
scholarrs727505352
googlers727505352
pharmgkbrs727505352
gwascentralrs727505352
openSNPrs727505352
23andMers727505352
23andMe allrs727505352
SNP Nexus

SNPshotrs727505352
SNPdbers727505352
MSV3drs727505352
GWAS Ctlgrs727505352
Max Magnitude0
ClinVar
Risk rs727505352(A,T;A,T)
Alt rs727505352(A,T;A,T)
Reference rs727505352(C;C)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179443562G>T
CLNSRC
CLNACC RCV000156911.1,