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rs794729339

From SNPedia

Orientationminus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs794729339(-;-)
Make rs794729339(-;AA)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178573283
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729339
ebirs794729339
HLIrs794729339
Exacrs794729339
Varsomers794729339
Maprs794729339
PheGenIrs794729339
hapmaprs794729339
1000 genomesrs794729339
hgdprs794729339
ensemblrs794729339
gopubmedrs794729339
geneviewrs794729339
scholarrs794729339
googlers794729339
pharmgkbrs794729339
gwascentralrs794729339
openSNPrs794729339
23andMers794729339
23andMe allrs794729339
SNP Nexus

SNPshotrs794729339
SNPdbers794729339
MSV3drs794729339
GWAS Ctlgrs794729339
Max Magnitude0
ClinVar
Risk rs794729339(;)
Alt rs794729339(;)
Reference rs794729339(AA;AA)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179438010_179438011delTT
CLNSRC
CLNACC RCV000184329.1,