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rs587777388

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587777388(A;A)
Make rs587777388(A;T)
ReferenceGRCh38 38.1/142
Chromosome2
Position73909088
GeneACTG2
is asnp
is mentioned by
dbSNPrs587777388
ebirs587777388
HLIrs587777388
Exacrs587777388
Varsomers587777388
Maprs587777388
PheGenIrs587777388
hapmaprs587777388
1000 genomesrs587777388
hgdprs587777388
ensemblrs587777388
gopubmedrs587777388
geneviewrs587777388
scholarrs587777388
googlers587777388
pharmgkbrs587777388
gwascentralrs587777388
openSNPrs587777388
23andMers587777388
23andMe allrs587777388
SNP Nexus

SNPshotrs587777388
SNPdbers587777388
MSV3drs587777388
GWAS Ctlgrs587777388
Max Magnitude0
ClinVar
Risk rs587777388(A;A)
Alt rs587777388(A;A)
Reference rs587777388(T;T)
Significance Pathogenic
Disease Visceral myopathy
Variation info
Gene ACTG2
CLNDBN Visceral myopathy
Reversed 0
HGVS NC_000002.11:g.74136215T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000119274.2,