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rs794729270

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794729270(A;A)
Make rs794729270(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178609489
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729270
ebirs794729270
HLIrs794729270
Exacrs794729270
Varsomers794729270
Maprs794729270
PheGenIrs794729270
hapmaprs794729270
1000 genomesrs794729270
hgdprs794729270
ensemblrs794729270
gopubmedrs794729270
geneviewrs794729270
scholarrs794729270
googlers794729270
pharmgkbrs794729270
gwascentralrs794729270
openSNPrs794729270
23andMers794729270
23andMe allrs794729270
SNP Nexus

SNPshotrs794729270
SNPdbers794729270
MSV3drs794729270
GWAS Ctlgrs794729270
Max Magnitude0
ClinVar
Risk rs794729270(A;A)
Alt rs794729270(A;A)
Reference rs794729270(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179474216G>T
CLNSRC
CLNACC RCV000184232.1,