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rs587777386

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777386(A;A)
Make rs587777386(A;G)
ReferenceGRCh38 38.1/142
Chromosome2
Position73901430
GeneACTG2
is asnp
is mentioned by
dbSNPrs587777386
ebirs587777386
HLIrs587777386
Exacrs587777386
Varsomers587777386
Maprs587777386
PheGenIrs587777386
hapmaprs587777386
1000 genomesrs587777386
hgdprs587777386
ensemblrs587777386
gopubmedrs587777386
geneviewrs587777386
scholarrs587777386
googlers587777386
pharmgkbrs587777386
gwascentralrs587777386
openSNPrs587777386
23andMers587777386
23andMe allrs587777386
SNP Nexus

SNPshotrs587777386
SNPdbers587777386
MSV3drs587777386
GWAS Ctlgrs587777386
Max Magnitude0
ClinVar
Risk rs587777386(A;A)
Alt rs587777386(A;A)
Reference rs587777386(G;G)
Significance Pathogenic
Disease Visceral myopathy
Variation info
Gene ACTG2
CLNDBN Visceral myopathy
Reversed 0
HGVS NC_000002.11:g.74128557G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000119271.2,