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rs878854373

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs878854373(A;A)
Make rs878854373(A;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178529958
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs878854373
ebirs878854373
HLIrs878854373
Exacrs878854373
Varsomers878854373
Maprs878854373
PheGenIrs878854373
hapmaprs878854373
1000 genomesrs878854373
hgdprs878854373
ensemblrs878854373
gopubmedrs878854373
geneviewrs878854373
scholarrs878854373
googlers878854373
pharmgkbrs878854373
gwascentralrs878854373
openSNPrs878854373
23andMers878854373
23andMe allrs878854373
SNP Nexus

SNPshotrs878854373
SNPdbers878854373
MSV3drs878854373
GWAS Ctlgrs878854373
Max Magnitude0
ClinVar
Risk rs878854373(A;A)
Alt rs878854373(A;A)
Reference rs878854373(T;T)
Significance Probable-Pathogenic
Disease Congenital muscular dystrophy
Variation info
Gene TTN TTN-AS1
CLNDBN Congenital muscular dystrophy
Reversed 1
HGVS NC_000002.11:g.179394685A>T
CLNSRC
CLNACC RCV000228738.1,