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rs794729319

From SNPedia

Orientationminus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs794729319(-;-)
Make rs794729319(-;AG)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178616873
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729319
ebirs794729319
HLIrs794729319
Exacrs794729319
Varsomers794729319
Maprs794729319
PheGenIrs794729319
hapmaprs794729319
1000 genomesrs794729319
hgdprs794729319
ensemblrs794729319
gopubmedrs794729319
geneviewrs794729319
scholarrs794729319
googlers794729319
pharmgkbrs794729319
gwascentralrs794729319
openSNPrs794729319
23andMers794729319
23andMe allrs794729319
SNP Nexus

SNPshotrs794729319
SNPdbers794729319
MSV3drs794729319
GWAS Ctlgrs794729319
Max Magnitude0
ClinVar
Risk rs794729319(;)
Alt rs794729319(;)
Reference rs794729319(AG;AG)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179481600_179481601delCT
CLNSRC
CLNACC RCV000184306.1,