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rs794729271

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794729271(A;A)
Make rs794729271(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178608410
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729271
ebirs794729271
HLIrs794729271
Exacrs794729271
Varsomers794729271
Maprs794729271
PheGenIrs794729271
hapmaprs794729271
1000 genomesrs794729271
hgdprs794729271
ensemblrs794729271
gopubmedrs794729271
geneviewrs794729271
scholarrs794729271
googlers794729271
pharmgkbrs794729271
gwascentralrs794729271
openSNPrs794729271
23andMers794729271
23andMe allrs794729271
SNP Nexus

SNPshotrs794729271
SNPdbers794729271
MSV3drs794729271
GWAS Ctlgrs794729271
Max Magnitude0
ClinVar
Risk rs794729271(A;A)
Alt rs794729271(A;A)
Reference rs794729271(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179473137C>T
CLNSRC
CLNACC RCV000184233.2,