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rs759231562

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs759231562(C;T)
Make rs759231562(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178607114
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs759231562
ebirs759231562
HLIrs759231562
Exacrs759231562
Varsomers759231562
Maprs759231562
PheGenIrs759231562
hapmaprs759231562
1000 genomesrs759231562
hgdprs759231562
ensemblrs759231562
gopubmedrs759231562
geneviewrs759231562
scholarrs759231562
googlers759231562
pharmgkbrs759231562
gwascentralrs759231562
openSNPrs759231562
23andMers759231562
23andMe allrs759231562
SNP Nexus

SNPshotrs759231562
SNPdbers759231562
MSV3drs759231562
GWAS Ctlgrs759231562
Max Magnitude0
ClinVar
Risk rs759231562(T;T)
Alt rs759231562(T;T)
Reference rs759231562(C;C)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000002.11:g.179471841C>A
CLNSRC
CLNACC RCV000209779.1,