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

rs745896785

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs745896785(C;T)
Make rs745896785(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178559457
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs745896785
ebirs745896785
HLIrs745896785
Exacrs745896785
Varsomers745896785
Maprs745896785
PheGenIrs745896785
hapmaprs745896785
1000 genomesrs745896785
hgdprs745896785
ensemblrs745896785
gopubmedrs745896785
geneviewrs745896785
scholarrs745896785
googlers745896785
pharmgkbrs745896785
gwascentralrs745896785
openSNPrs745896785
23andMers745896785
23andMe allrs745896785
SNP Nexus

SNPshotrs745896785
SNPdbers745896785
MSV3drs745896785
GWAS Ctlgrs745896785
Max Magnitude0
ClinVar
Risk rs745896785(G,T;G,T)
Alt rs745896785(G,T;G,T)
Reference rs745896785(C;C)
Significance Probable-Pathogenic
Disease Dilated cardiomyopathy 1G
Variation info
Gene TTN TTN-AS1
CLNDBN Dilated cardiomyopathy 1G
Reversed 0
HGVS NC_000002.11:g.179424184C>T
CLNSRC
CLNACC RCV000234586.1,