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rs878854370

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs878854370(A;G)
Make rs878854370(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178651450
GeneTTN
is asnp
is mentioned by
dbSNPrs878854370
ebirs878854370
HLIrs878854370
Exacrs878854370
Varsomers878854370
Maprs878854370
PheGenIrs878854370
hapmaprs878854370
1000 genomesrs878854370
hgdprs878854370
ensemblrs878854370
gopubmedrs878854370
geneviewrs878854370
scholarrs878854370
googlers878854370
pharmgkbrs878854370
gwascentralrs878854370
openSNPrs878854370
23andMers878854370
23andMe allrs878854370
SNP Nexus

SNPshotrs878854370
SNPdbers878854370
MSV3drs878854370
GWAS Ctlgrs878854370
Max Magnitude0
ClinVar
Risk rs878854370(G;G)
Alt rs878854370(G;G)
Reference rs878854370(A;A)
Significance Probable-Pathogenic
Disease Congenital muscular dystrophy
Variation info
Gene TTN
CLNDBN Congenital muscular dystrophy
Reversed 1
HGVS NC_000002.11:g.179516177T>C
CLNSRC
CLNACC RCV000226930.1,