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rs794729348

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794729348(-;-)
Make rs794729348(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178565548
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729348
ebirs794729348
HLIrs794729348
Exacrs794729348
Varsomers794729348
Maprs794729348
PheGenIrs794729348
hapmaprs794729348
1000 genomesrs794729348
hgdprs794729348
ensemblrs794729348
gopubmedrs794729348
geneviewrs794729348
scholarrs794729348
googlers794729348
pharmgkbrs794729348
gwascentralrs794729348
openSNPrs794729348
23andMers794729348
23andMe allrs794729348
SNP Nexus

SNPshotrs794729348
SNPdbers794729348
MSV3drs794729348
GWAS Ctlgrs794729348
Max Magnitude0
ClinVar
Risk rs794729348(;)
Alt rs794729348(;)
Reference rs794729348(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179430275delT
CLNSRC
CLNACC RCV000184339.1,