Have questions? Visit https://www.reddit.com/r/SNPedia

rs727503567

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727503567(A;A)
Make rs727503567(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position178574811
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs727503567
ebirs727503567
HLIrs727503567
Exacrs727503567
Varsomers727503567
Maprs727503567
PheGenIrs727503567
hapmaprs727503567
1000 genomesrs727503567
hgdprs727503567
ensemblrs727503567
gopubmedrs727503567
geneviewrs727503567
scholarrs727503567
googlers727503567
pharmgkbrs727503567
gwascentralrs727503567
openSNPrs727503567
23andMers727503567
23andMe allrs727503567
SNP Nexus

SNPshotrs727503567
SNPdbers727503567
MSV3drs727503567
GWAS Ctlgrs727503567
Max Magnitude0
ClinVar
Risk rs727503567(A;A)
Alt rs727503567(A;A)
Reference rs727503567(G;G)
Significance Pathogenic
Disease Primary dilated cardiomyopathy not provided
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy not provided
Reversed 1
HGVS NC_000002.11:g.179439538C>T
CLNSRC
CLNACC RCV000152227.1, RCV000184257.2,