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

rs794729352

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794729352(-;-)
Make rs794729352(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178562073
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729352
ebirs794729352
HLIrs794729352
Exacrs794729352
Varsomers794729352
Maprs794729352
PheGenIrs794729352
hapmaprs794729352
1000 genomesrs794729352
hgdprs794729352
ensemblrs794729352
gopubmedrs794729352
geneviewrs794729352
scholarrs794729352
googlers794729352
pharmgkbrs794729352
gwascentralrs794729352
openSNPrs794729352
23andMers794729352
23andMe allrs794729352
SNP Nexus

SNPshotrs794729352
SNPdbers794729352
MSV3drs794729352
GWAS Ctlgrs794729352
Max Magnitude0
ClinVar
Risk rs794729352(;)
Alt rs794729352(;)
Reference rs794729352(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179426800delA
CLNSRC
CLNACC RCV000184345.1,