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rs864309491

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs864309491(C;G)
Make rs864309491(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position73902420
GeneACTG2
is asnp
is mentioned by
dbSNPrs864309491
ebirs864309491
HLIrs864309491
Exacrs864309491
Varsomers864309491
Maprs864309491
PheGenIrs864309491
hapmaprs864309491
1000 genomesrs864309491
hgdprs864309491
ensemblrs864309491
gopubmedrs864309491
geneviewrs864309491
scholarrs864309491
googlers864309491
pharmgkbrs864309491
gwascentralrs864309491
openSNPrs864309491
23andMers864309491
23andMe allrs864309491
SNP Nexus

SNPshotrs864309491
SNPdbers864309491
MSV3drs864309491
GWAS Ctlgrs864309491
Max Magnitude0
ClinVar
Risk rs864309491(G;G)
Alt rs864309491(G;G)
Reference rs864309491(C;C)
Significance Pathogenic
Disease Visceral myopathy
Variation info
Gene ACTG2
CLNDBN Visceral myopathy
Reversed 0
HGVS NC_000002.11:g.74129547C>G
CLNSRC
CLNACC RCV000202512.1,