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rs794729287

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794729287(C;T)
Make rs794729287(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178568695
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729287
ebirs794729287
HLIrs794729287
Exacrs794729287
Varsomers794729287
Maprs794729287
PheGenIrs794729287
hapmaprs794729287
1000 genomesrs794729287
hgdprs794729287
ensemblrs794729287
gopubmedrs794729287
geneviewrs794729287
scholarrs794729287
googlers794729287
pharmgkbrs794729287
gwascentralrs794729287
openSNPrs794729287
23andMers794729287
23andMe allrs794729287
SNP Nexus

SNPshotrs794729287
SNPdbers794729287
MSV3drs794729287
GWAS Ctlgrs794729287
Max Magnitude0
ClinVar
Risk rs794729287(T;T)
Alt rs794729287(T;T)
Reference rs794729287(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179433422G>A
CLNSRC
CLNACC RCV000184263.1,