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

rs794729300

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794729300(A;T)
Make rs794729300(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178554510
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729300
ClinGenrs794729300
ebirs794729300
HLIrs794729300
Exacrs794729300
Varsomers794729300
Maprs794729300
PheGenIrs794729300
hapmaprs794729300
1000 genomesrs794729300
hgdprs794729300
ensemblrs794729300
gopubmedrs794729300
geneviewrs794729300
scholarrs794729300
googlers794729300
pharmgkbrs794729300
gwascentralrs794729300
openSNPrs794729300
23andMers794729300
23andMe allrs794729300
SNP Nexus

SNPshotrs794729300
SNPdbers794729300
MSV3drs794729300
GWAS Ctlgrs794729300
Max Magnitude0
ClinVar
Risk rs794729300(T;T)
Alt rs794729300(T;T)
Reference Rs794729300(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179419237T>A
CLNSRC
CLNACC RCV000184280.1,