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rs794729359

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794729359(-;-)
Make rs794729359(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178557414
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729359
ebirs794729359
HLIrs794729359
Exacrs794729359
Varsomers794729359
Maprs794729359
PheGenIrs794729359
hapmaprs794729359
1000 genomesrs794729359
hgdprs794729359
ensemblrs794729359
gopubmedrs794729359
geneviewrs794729359
scholarrs794729359
googlers794729359
pharmgkbrs794729359
gwascentralrs794729359
openSNPrs794729359
23andMers794729359
23andMe allrs794729359
SNP Nexus

SNPshotrs794729359
SNPdbers794729359
MSV3drs794729359
GWAS Ctlgrs794729359
Max Magnitude0
ClinVar
Risk rs794729359(;)
Alt rs794729359(;)
Reference rs794729359(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179422141delA
CLNSRC
CLNACC RCV000184352.1,