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

rs794729267

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794729267(G;T)
Make rs794729267(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178611408
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729267
ebirs794729267
HLIrs794729267
Exacrs794729267
Varsomers794729267
Maprs794729267
PheGenIrs794729267
hapmaprs794729267
1000 genomesrs794729267
hgdprs794729267
ensemblrs794729267
gopubmedrs794729267
geneviewrs794729267
scholarrs794729267
googlers794729267
pharmgkbrs794729267
gwascentralrs794729267
openSNPrs794729267
23andMers794729267
23andMe allrs794729267
SNP Nexus

SNPshotrs794729267
SNPdbers794729267
MSV3drs794729267
GWAS Ctlgrs794729267
Max Magnitude0
ClinVar
Risk rs794729267(T;T)
Alt rs794729267(T;T)
Reference rs794729267(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179476135C>A
CLNSRC
CLNACC RCV000184228.1,