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rs864309490

From SNPedia

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Geno Mag Summary
(T;T) 0 common in clinvar
Make rs864309490(C;C)
Make rs864309490(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position73902367
GeneACTG2
is asnp
is mentioned by
dbSNPrs864309490
ebirs864309490
HLIrs864309490
Exacrs864309490
Varsomers864309490
Maprs864309490
PheGenIrs864309490
hapmaprs864309490
1000 genomesrs864309490
hgdprs864309490
ensemblrs864309490
gopubmedrs864309490
geneviewrs864309490
scholarrs864309490
googlers864309490
pharmgkbrs864309490
gwascentralrs864309490
openSNPrs864309490
23andMers864309490
23andMe allrs864309490
SNP Nexus

SNPshotrs864309490
SNPdbers864309490
MSV3drs864309490
GWAS Ctlgrs864309490
Max Magnitude0
ClinVar
Risk rs864309490(C;C)
Alt rs864309490(C;C)
Reference rs864309490(T;T)
Significance Pathogenic
Disease Visceral myopathy
Variation info
Gene ACTG2
CLNDBN Visceral myopathy
Reversed 0
HGVS NC_000002.11:g.74129494T>C
CLNSRC
CLNACC RCV000202556.1,