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rs753334568

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs753334568(A;A)
Make rs753334568(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178546041
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs753334568
ebirs753334568
HLIrs753334568
Exacrs753334568
Varsomers753334568
Maprs753334568
PheGenIrs753334568
hapmaprs753334568
1000 genomesrs753334568
hgdprs753334568
ensemblrs753334568
gopubmedrs753334568
geneviewrs753334568
scholarrs753334568
googlers753334568
pharmgkbrs753334568
gwascentralrs753334568
openSNPrs753334568
23andMers753334568
23andMe allrs753334568
SNP Nexus

SNPshotrs753334568
SNPdbers753334568
MSV3drs753334568
GWAS Ctlgrs753334568
Max Magnitude0
ClinVar
Risk rs753334568(A;A)
Alt rs753334568(A;A)
Reference rs753334568(G;G)
Significance Pathogenic
Disease Hereditary myopathy with early respiratory failure
Variation info
Gene TTN TTN-AS1
CLNDBN Hereditary myopathy with early respiratory failure
Reversed 0
HGVS NC_000002.11:g.179410768G>A
CLNSRC
CLNACC RCV000119025.2,