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rs794729264

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794729264(C;G)
Make rs794729264(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178612858
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729264
ebirs794729264
HLIrs794729264
Exacrs794729264
Varsomers794729264
Maprs794729264
PheGenIrs794729264
hapmaprs794729264
1000 genomesrs794729264
hgdprs794729264
ensemblrs794729264
gopubmedrs794729264
geneviewrs794729264
scholarrs794729264
googlers794729264
pharmgkbrs794729264
gwascentralrs794729264
openSNPrs794729264
23andMers794729264
23andMe allrs794729264
SNP Nexus

SNPshotrs794729264
SNPdbers794729264
MSV3drs794729264
GWAS Ctlgrs794729264
Max Magnitude0
ClinVar
Risk rs794729264(G;G)
Alt rs794729264(G;G)
Reference rs794729264(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179477585G>C
CLNSRC
CLNACC RCV000184222.1,