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rs878854377

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878854377(C;C)
Make rs878854377(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178601260
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs878854377
ebirs878854377
HLIrs878854377
Exacrs878854377
Varsomers878854377
Maprs878854377
PheGenIrs878854377
hapmaprs878854377
1000 genomesrs878854377
hgdprs878854377
ensemblrs878854377
gopubmedrs878854377
geneviewrs878854377
scholarrs878854377
googlers878854377
pharmgkbrs878854377
gwascentralrs878854377
openSNPrs878854377
23andMers878854377
23andMe allrs878854377
SNP Nexus

SNPshotrs878854377
SNPdbers878854377
MSV3drs878854377
GWAS Ctlgrs878854377
Max Magnitude0
ClinVar
Risk rs878854377(C;C)
Alt rs878854377(C;C)
Reference rs878854377(G;G)
Significance Probable-Pathogenic
Disease Limb-girdle muscular dystrophy
Variation info
Gene TTN TTN-AS1
CLNDBN Limb-girdle muscular dystrophy, type 2J
Reversed 1
HGVS NC_000002.11:g.179465987C>G
CLNSRC
CLNACC RCV000228520.1,