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rs794729297

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794729297(G;G)
Make rs794729297(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178559658
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729297
ebirs794729297
HLIrs794729297
Exacrs794729297
Varsomers794729297
Maprs794729297
PheGenIrs794729297
hapmaprs794729297
1000 genomesrs794729297
hgdprs794729297
ensemblrs794729297
gopubmedrs794729297
geneviewrs794729297
scholarrs794729297
googlers794729297
pharmgkbrs794729297
gwascentralrs794729297
openSNPrs794729297
23andMers794729297
23andMe allrs794729297
SNP Nexus

SNPshotrs794729297
SNPdbers794729297
MSV3drs794729297
GWAS Ctlgrs794729297
Max Magnitude0
ClinVar
Risk rs794729297(G;G)
Alt rs794729297(G;G)
Reference rs794729297(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179424385A>C
CLNSRC
CLNACC RCV000184276.2,