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rs794729268

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794729268(A;T)
Make rs794729268(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178611269
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729268
ebirs794729268
HLIrs794729268
Exacrs794729268
Varsomers794729268
Maprs794729268
PheGenIrs794729268
hapmaprs794729268
1000 genomesrs794729268
hgdprs794729268
ensemblrs794729268
gopubmedrs794729268
geneviewrs794729268
scholarrs794729268
googlers794729268
pharmgkbrs794729268
gwascentralrs794729268
openSNPrs794729268
23andMers794729268
23andMe allrs794729268
SNP Nexus

SNPshotrs794729268
SNPdbers794729268
MSV3drs794729268
GWAS Ctlgrs794729268
Max Magnitude0
ClinVar
Risk rs794729268(T;T)
Alt rs794729268(T;T)
Reference rs794729268(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179475996T>A
CLNSRC
CLNACC RCV000184229.1,