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rs794729299

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794729299(C;T)
Make rs794729299(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178557511
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729299
ebirs794729299
HLIrs794729299
Exacrs794729299
Varsomers794729299
Maprs794729299
PheGenIrs794729299
hapmaprs794729299
1000 genomesrs794729299
hgdprs794729299
ensemblrs794729299
gopubmedrs794729299
geneviewrs794729299
scholarrs794729299
googlers794729299
pharmgkbrs794729299
gwascentralrs794729299
openSNPrs794729299
23andMers794729299
23andMe allrs794729299
SNP Nexus

SNPshotrs794729299
SNPdbers794729299
MSV3drs794729299
GWAS Ctlgrs794729299
Max Magnitude0
ClinVar
Risk rs794729299(T;T)
Alt rs794729299(T;T)
Reference rs794729299(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179422238G>A
CLNSRC
CLNACC RCV000184279.1,