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rs794729269

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794729269(A;T)
Make rs794729269(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178611002
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729269
ebirs794729269
HLIrs794729269
Exacrs794729269
Varsomers794729269
Maprs794729269
PheGenIrs794729269
hapmaprs794729269
1000 genomesrs794729269
hgdprs794729269
ensemblrs794729269
gopubmedrs794729269
geneviewrs794729269
scholarrs794729269
googlers794729269
pharmgkbrs794729269
gwascentralrs794729269
openSNPrs794729269
23andMers794729269
23andMe allrs794729269
SNP Nexus

SNPshotrs794729269
SNPdbers794729269
MSV3drs794729269
GWAS Ctlgrs794729269
Max Magnitude0
ClinVar
Risk rs794729269(C;C)
Alt rs794729269(C;C)
Reference rs794729269(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179475729T>A
CLNSRC
CLNACC RCV000184230.1,