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rs794729337

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794729337(-;-)
Make rs794729337(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178574493
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729337
ebirs794729337
HLIrs794729337
Exacrs794729337
Varsomers794729337
Maprs794729337
PheGenIrs794729337
hapmaprs794729337
1000 genomesrs794729337
hgdprs794729337
ensemblrs794729337
gopubmedrs794729337
geneviewrs794729337
scholarrs794729337
googlers794729337
pharmgkbrs794729337
gwascentralrs794729337
openSNPrs794729337
23andMers794729337
23andMe allrs794729337
SNP Nexus

SNPshotrs794729337
SNPdbers794729337
MSV3drs794729337
GWAS Ctlgrs794729337
Max Magnitude0
ClinVar
Risk rs794729337(;)
Alt rs794729337(;)
Reference rs794729337(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179439220delA
CLNSRC
CLNACC RCV000184326.1,