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rs727504782

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727504782(-;-)
Make rs727504782(-;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position178562725
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs727504782
ebirs727504782
HLIrs727504782
Exacrs727504782
Varsomers727504782
Maprs727504782
PheGenIrs727504782
hapmaprs727504782
1000 genomesrs727504782
hgdprs727504782
ensemblrs727504782
gopubmedrs727504782
geneviewrs727504782
scholarrs727504782
googlers727504782
pharmgkbrs727504782
gwascentralrs727504782
openSNPrs727504782
23andMers727504782
23andMe allrs727504782
SNP Nexus

SNPshotrs727504782
SNPdbers727504782
MSV3drs727504782
GWAS Ctlgrs727504782
Max Magnitude0
ClinVar
Risk rs727504782(;)
Alt rs727504782(;)
Reference rs727504782(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.179427452delC
CLNSRC
CLNACC RCV000156100.1,