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rs878854363

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs878854363(C;C)
Make rs878854363(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome9
Position35689205
GeneTPM2
is asnp
is mentioned by
dbSNPrs878854363
ebirs878854363
HLIrs878854363
Exacrs878854363
Varsomers878854363
Maprs878854363
PheGenIrs878854363
hapmaprs878854363
1000 genomesrs878854363
hgdprs878854363
ensemblrs878854363
gopubmedrs878854363
geneviewrs878854363
scholarrs878854363
googlers878854363
pharmgkbrs878854363
gwascentralrs878854363
openSNPrs878854363
23andMers878854363
23andMe allrs878854363
SNP Nexus

SNPshotrs878854363
SNPdbers878854363
MSV3drs878854363
GWAS Ctlgrs878854363
Max Magnitude0
ClinVar
Risk rs878854363(C;C)
Alt rs878854363(C;C)
Reference rs878854363(T;T)
Significance Probable-Pathogenic
Disease Nemaline myopathy 4
Variation info
Gene TPM2
CLNDBN Nemaline myopathy 4
Reversed 1
HGVS NC_000009.11:g.35689202A>G
CLNSRC
CLNACC RCV000234310.1,