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rs794729356

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794729356(-;-)
Make rs794729356(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178557999
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729356
ebirs794729356
HLIrs794729356
Exacrs794729356
Varsomers794729356
Maprs794729356
PheGenIrs794729356
hapmaprs794729356
1000 genomesrs794729356
hgdprs794729356
ensemblrs794729356
gopubmedrs794729356
geneviewrs794729356
scholarrs794729356
googlers794729356
pharmgkbrs794729356
gwascentralrs794729356
openSNPrs794729356
23andMers794729356
23andMe allrs794729356
SNP Nexus

SNPshotrs794729356
SNPdbers794729356
MSV3drs794729356
GWAS Ctlgrs794729356
Max Magnitude0
ClinVar
Risk rs794729356(;)
Alt rs794729356(;)
Reference rs794729356(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179422726delC
CLNSRC
CLNACC RCV000184349.2,