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rs794729385

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794729385(A;A)
Make rs794729385(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178553725
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729385
ebirs794729385
HLIrs794729385
Exacrs794729385
Varsomers794729385
Maprs794729385
PheGenIrs794729385
hapmaprs794729385
1000 genomesrs794729385
hgdprs794729385
ensemblrs794729385
gopubmedrs794729385
geneviewrs794729385
scholarrs794729385
googlers794729385
pharmgkbrs794729385
gwascentralrs794729385
openSNPrs794729385
23andMers794729385
23andMe allrs794729385
SNP Nexus

SNPshotrs794729385
SNPdbers794729385
MSV3drs794729385
GWAS Ctlgrs794729385
Max Magnitude0
ClinVar
Risk rs794729385(A;A)
Alt rs794729385(A;A)
Reference rs794729385(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179418452A>T
CLNSRC
CLNACC RCV000184395.2,