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rs876661407

From SNPedia

Orientationminus
Geno Mag Summary
(AGA;AGA) 0 common in clinvar
Make rs876661407(-;-)
Make rs876661407(-;AGA)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position154170695
GeneTPM3
is asnp
is mentioned by
dbSNPrs876661407
ebirs876661407
HLIrs876661407
Exacrs876661407
Varsomers876661407
Maprs876661407
PheGenIrs876661407
hapmaprs876661407
1000 genomesrs876661407
hgdprs876661407
ensemblrs876661407
gopubmedrs876661407
geneviewrs876661407
scholarrs876661407
googlers876661407
pharmgkbrs876661407
gwascentralrs876661407
openSNPrs876661407
23andMers876661407
23andMe allrs876661407
SNP Nexus

SNPshotrs876661407
SNPdbers876661407
MSV3drs876661407
GWAS Ctlgrs876661407
Max Magnitude0
ClinVar
Risk rs876661407(;)
Alt rs876661407(;)
Reference rs876661407(AGA;AGA)
Significance Pathogenic
Disease Nemaline myopathy 1
Variation info
Gene TPM3
CLNDBN Nemaline myopathy 1
Reversed 1
HGVS NC_000001.10:g.154143171_154143173delTCT
CLNSRC OMIM Allelic Variant
CLNACC RCV000223955.1,