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rs755261062

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs755261062(-;-)
Make rs755261062(-;A)
Make rs755261062(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178592593
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs755261062
ebirs755261062
HLIrs755261062
Exacrs755261062
Varsomers755261062
Maprs755261062
PheGenIrs755261062
hapmaprs755261062
1000 genomesrs755261062
hgdprs755261062
ensemblrs755261062
gopubmedrs755261062
geneviewrs755261062
scholarrs755261062
googlers755261062
pharmgkbrs755261062
gwascentralrs755261062
openSNPrs755261062
23andMers755261062
23andMe allrs755261062
SNP Nexus

SNPshotrs755261062
SNPdbers755261062
MSV3drs755261062
GWAS Ctlgrs755261062
Max Magnitude0
ClinVar
Risk rs755261062(A;A)
Alt rs755261062(A;A)
Reference rs755261062(;)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000002.11:g.179457321dupA
CLNSRC
CLNACC RCV000209014.1,