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rs794729383

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794729383(A;A)
Make rs794729383(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178569501
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729383
ebirs794729383
HLIrs794729383
Exacrs794729383
Varsomers794729383
Maprs794729383
PheGenIrs794729383
hapmaprs794729383
1000 genomesrs794729383
hgdprs794729383
ensemblrs794729383
gopubmedrs794729383
geneviewrs794729383
scholarrs794729383
googlers794729383
pharmgkbrs794729383
gwascentralrs794729383
openSNPrs794729383
23andMers794729383
23andMe allrs794729383
SNP Nexus

SNPshotrs794729383
SNPdbers794729383
MSV3drs794729383
GWAS Ctlgrs794729383
Max Magnitude0
ClinVar
Risk rs794729383(A;A)
Alt rs794729383(A;A)
Reference rs794729383(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179434228C>T
CLNSRC
CLNACC RCV000184391.2,