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rs876661406

From SNPedia

Orientationminus
Geno Mag Summary
(GAA;GAA) 0 common in clinvar
Make rs876661406(-;-)
Make rs876661406(-;GAA)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position154170679
GeneTPM3
is asnp
is mentioned by
dbSNPrs876661406
ebirs876661406
HLIrs876661406
Exacrs876661406
Varsomers876661406
Maprs876661406
PheGenIrs876661406
hapmaprs876661406
1000 genomesrs876661406
hgdprs876661406
ensemblrs876661406
gopubmedrs876661406
geneviewrs876661406
scholarrs876661406
googlers876661406
pharmgkbrs876661406
gwascentralrs876661406
openSNPrs876661406
23andMers876661406
23andMe allrs876661406
SNP Nexus

SNPshotrs876661406
SNPdbers876661406
MSV3drs876661406
GWAS Ctlgrs876661406
Max Magnitude0
ClinVar
Risk rs876661406(;)
Alt rs876661406(;)
Reference rs876661406(GAA;GAA)
Significance Pathogenic
Disease Nemaline myopathy 1
Variation info
Gene TPM3
CLNDBN Nemaline myopathy 1
Reversed 1
HGVS NC_000001.10:g.154143155_154143157delTTC
CLNSRC OMIM Allelic Variant
CLNACC RCV000223952.1,