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rs794729302

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794729302(A;T)
Make rs794729302(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178547464
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729302
ebirs794729302
HLIrs794729302
Exacrs794729302
Varsomers794729302
Maprs794729302
PheGenIrs794729302
hapmaprs794729302
1000 genomesrs794729302
hgdprs794729302
ensemblrs794729302
gopubmedrs794729302
geneviewrs794729302
scholarrs794729302
googlers794729302
pharmgkbrs794729302
gwascentralrs794729302
openSNPrs794729302
23andMers794729302
23andMe allrs794729302
SNP Nexus

SNPshotrs794729302
SNPdbers794729302
MSV3drs794729302
GWAS Ctlgrs794729302
Max Magnitude0
ClinVar
Risk rs794729302(T;T)
Alt rs794729302(T;T)
Reference rs794729302(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179412191T>A
CLNSRC
CLNACC RCV000184282.1,