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rs727504499

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727504499(C;T)
Make rs727504499(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position178632294
GeneTTN
is asnp
is mentioned by
dbSNPrs727504499
ebirs727504499
HLIrs727504499
Exacrs727504499
Varsomers727504499
Maprs727504499
PheGenIrs727504499
hapmaprs727504499
1000 genomesrs727504499
hgdprs727504499
ensemblrs727504499
gopubmedrs727504499
geneviewrs727504499
scholarrs727504499
googlers727504499
pharmgkbrs727504499
gwascentralrs727504499
openSNPrs727504499
23andMers727504499
23andMe allrs727504499
SNP Nexus

SNPshotrs727504499
SNPdbers727504499
MSV3drs727504499
GWAS Ctlgrs727504499
Max Magnitude0
ClinVar
Risk rs727504499(T;T)
Alt rs727504499(T;T)
Reference rs727504499(C;C)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy not specified
Variation info
Gene TTN
CLNDBN Primary dilated cardiomyopathy not specified
Reversed 1
HGVS NC_000002.11:g.179497021G>A
CLNSRC
CLNACC RCV000155637.2, RCV000184210.2,