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rs864309492

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs864309492(A;A)
Make rs864309492(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position73913626
GeneACTG2
is asnp
is mentioned by
dbSNPrs864309492
ebirs864309492
HLIrs864309492
Exacrs864309492
Varsomers864309492
Maprs864309492
PheGenIrs864309492
hapmaprs864309492
1000 genomesrs864309492
hgdprs864309492
ensemblrs864309492
gopubmedrs864309492
geneviewrs864309492
scholarrs864309492
googlers864309492
pharmgkbrs864309492
gwascentralrs864309492
openSNPrs864309492
23andMers864309492
23andMe allrs864309492
SNP Nexus

SNPshotrs864309492
SNPdbers864309492
MSV3drs864309492
GWAS Ctlgrs864309492
Max Magnitude0
ClinVar
Risk rs864309492(A;A)
Alt rs864309492(A;A)
Reference rs864309492(G;G)
Significance Pathogenic
Disease Visceral myopathy
Variation info
Gene ACTG2
CLNDBN Visceral myopathy
Reversed 0
HGVS NC_000002.11:g.74140753G>A
CLNSRC
CLNACC RCV000202479.1,