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rs794729333

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794729333(-;-)
Make rs794729333(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178576599
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729333
ebirs794729333
HLIrs794729333
Exacrs794729333
Varsomers794729333
Maprs794729333
PheGenIrs794729333
hapmaprs794729333
1000 genomesrs794729333
hgdprs794729333
ensemblrs794729333
gopubmedrs794729333
geneviewrs794729333
scholarrs794729333
googlers794729333
pharmgkbrs794729333
gwascentralrs794729333
openSNPrs794729333
23andMers794729333
23andMe allrs794729333
SNP Nexus

SNPshotrs794729333
SNPdbers794729333
MSV3drs794729333
GWAS Ctlgrs794729333
Max Magnitude0
ClinVar
Risk rs794729333(;)
Alt rs794729333(;)
Reference rs794729333(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179441326delA
CLNSRC
CLNACC RCV000184322.1,