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rs794729334

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs794729334(-;-)
Make rs794729334(-;A)
Make rs794729334(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178576588
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729334
ebirs794729334
HLIrs794729334
Exacrs794729334
Varsomers794729334
Maprs794729334
PheGenIrs794729334
hapmaprs794729334
1000 genomesrs794729334
hgdprs794729334
ensemblrs794729334
gopubmedrs794729334
geneviewrs794729334
scholarrs794729334
googlers794729334
pharmgkbrs794729334
gwascentralrs794729334
openSNPrs794729334
23andMers794729334
23andMe allrs794729334
SNP Nexus

SNPshotrs794729334
SNPdbers794729334
MSV3drs794729334
GWAS Ctlgrs794729334
Max Magnitude0
ClinVar
Risk rs794729334(A;A)
Alt rs794729334(A;A)
Reference rs794729334(;)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179441316dupT
CLNSRC
CLNACC RCV000184323.1,