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rs794729305

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794729305(C;T)
Make rs794729305(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178535388
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729305
ebirs794729305
HLIrs794729305
Exacrs794729305
Varsomers794729305
Maprs794729305
PheGenIrs794729305
hapmaprs794729305
1000 genomesrs794729305
hgdprs794729305
ensemblrs794729305
gopubmedrs794729305
geneviewrs794729305
scholarrs794729305
googlers794729305
pharmgkbrs794729305
gwascentralrs794729305
openSNPrs794729305
23andMers794729305
23andMe allrs794729305
SNP Nexus

SNPshotrs794729305
SNPdbers794729305
MSV3drs794729305
GWAS Ctlgrs794729305
Max Magnitude0
ClinVar
Risk rs794729305(T;T)
Alt rs794729305(T;T)
Reference rs794729305(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179400115G>A
CLNSRC
CLNACC RCV000184287.1,