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rs727503697

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727503697(C;T)
Make rs727503697(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position178779055
GeneLOC101927055, TTN
is asnp
is mentioned by
dbSNPrs727503697
ebirs727503697
HLIrs727503697
Exacrs727503697
Varsomers727503697
Maprs727503697
PheGenIrs727503697
hapmaprs727503697
1000 genomesrs727503697
hgdprs727503697
ensemblrs727503697
gopubmedrs727503697
geneviewrs727503697
scholarrs727503697
googlers727503697
pharmgkbrs727503697
gwascentralrs727503697
openSNPrs727503697
23andMers727503697
23andMe allrs727503697
SNP Nexus

SNPshotrs727503697
SNPdbers727503697
MSV3drs727503697
GWAS Ctlgrs727503697
Max Magnitude0
ClinVar
Risk rs727503697(T;T)
Alt rs727503697(T;T)
Reference rs727503697(C;C)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN LOC101927055
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179643782G>A
CLNSRC
CLNACC RCV000152508.1,