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

rs794729353

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GAGAGTGT;GAGAGTGT) 0 common in clinvar
Make rs794729353(-;-)
Make rs794729353(-;GAGAGTGT)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178560513
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729353
dbSNP (classic)rs794729353
ClinGenrs794729353
ebirs794729353
HLIrs794729353
Exacrs794729353
Gnomadrs794729353
Varsomers794729353
LitVarrs794729353
Maprs794729353
PheGenIrs794729353
Biobankrs794729353
1000 genomesrs794729353
hgdprs794729353
ensemblrs794729353
geneviewrs794729353
scholarrs794729353
googlers794729353
pharmgkbrs794729353
gwascentralrs794729353
openSNPrs794729353
23andMers794729353
SNPshotrs794729353
SNPdbers794729353
MSV3drs794729353
GWAS Ctlgrs794729353
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs794729353(GAGAGTGT;GAGAGTGT)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179425240_179425247delACACTCTC
CLNSRC
CLNACC RCV000184346.1,