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rs768290597

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs768290597(A;A)
Make rs768290597(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position73902698
GeneACTG2
is asnp
is mentioned by
dbSNPrs768290597
ebirs768290597
HLIrs768290597
Exacrs768290597
Varsomers768290597
Maprs768290597
PheGenIrs768290597
hapmaprs768290597
1000 genomesrs768290597
hgdprs768290597
ensemblrs768290597
gopubmedrs768290597
geneviewrs768290597
scholarrs768290597
googlers768290597
pharmgkbrs768290597
gwascentralrs768290597
openSNPrs768290597
23andMers768290597
23andMe allrs768290597
SNP Nexus

SNPshotrs768290597
SNPdbers768290597
MSV3drs768290597
GWAS Ctlgrs768290597
Max Magnitude0
ClinVar
Risk rs768290597(A;A)
Alt rs768290597(A;A)
Reference rs768290597(C;C)
Significance Pathogenic
Disease Visceral myopathy
Variation info
Gene ACTG2
CLNDBN Visceral myopathy
Reversed 0
HGVS NC_000002.11:g.74129825C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000202559.2,