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rs587777301

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587777301(A;G)
Make rs587777301(G;G)
ReferenceGRCh38 38.1/142
Chromosome5
Position139322683
GeneMATR3
is asnp
is mentioned by
dbSNPrs587777301
ebirs587777301
HLIrs587777301
Exacrs587777301
Varsomers587777301
Maprs587777301
PheGenIrs587777301
hapmaprs587777301
1000 genomesrs587777301
hgdprs587777301
ensemblrs587777301
gopubmedrs587777301
geneviewrs587777301
scholarrs587777301
googlers587777301
pharmgkbrs587777301
gwascentralrs587777301
openSNPrs587777301
23andMers587777301
23andMe allrs587777301
SNP Nexus

SNPshotrs587777301
SNPdbers587777301
MSV3drs587777301
GWAS Ctlgrs587777301
Max Magnitude0
ClinVar
Risk rs587777301(G;G)
Alt rs587777301(G;G)
Reference rs587777301(A;A)
Significance Pathogenic
Disease Myopathy
Variation info
Gene MATR3
CLNDBN Myopathy, distal, 2
Reversed 0
HGVS NC_000005.9:g.138658372A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000114431.3,