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rs727503598

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727503598(A;A)
Make rs727503598(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position178601104
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs727503598
ebirs727503598
HLIrs727503598
Exacrs727503598
Varsomers727503598
Maprs727503598
PheGenIrs727503598
hapmaprs727503598
1000 genomesrs727503598
hgdprs727503598
ensemblrs727503598
gopubmedrs727503598
geneviewrs727503598
scholarrs727503598
googlers727503598
pharmgkbrs727503598
gwascentralrs727503598
openSNPrs727503598
23andMers727503598
23andMe allrs727503598
SNP Nexus

SNPshotrs727503598
SNPdbers727503598
MSV3drs727503598
GWAS Ctlgrs727503598
Max Magnitude0
ClinVar
Risk rs727503598(A;A)
Alt rs727503598(A;A)
Reference rs727503598(G;G)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179465831C>T
CLNSRC
CLNACC RCV000152296.1,