Have questions? Visit https://www.reddit.com/r/SNPedia

rs794729325

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794729325(-;-)
Make rs794729325(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178605065
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729325
ebirs794729325
HLIrs794729325
Exacrs794729325
Varsomers794729325
Maprs794729325
PheGenIrs794729325
hapmaprs794729325
1000 genomesrs794729325
hgdprs794729325
ensemblrs794729325
gopubmedrs794729325
geneviewrs794729325
scholarrs794729325
googlers794729325
pharmgkbrs794729325
gwascentralrs794729325
openSNPrs794729325
23andMers794729325
23andMe allrs794729325
SNP Nexus

SNPshotrs794729325
SNPdbers794729325
MSV3drs794729325
GWAS Ctlgrs794729325
Max Magnitude0
ClinVar
Risk rs794729325(;)
Alt rs794729325(;)
Reference rs794729325(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179469792delC
CLNSRC
CLNACC RCV000184313.1,