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rs794728966

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728966(A;A)
Make rs794728966(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position236762460
GeneACTN2
is asnp
is mentioned by
dbSNPrs794728966
ebirs794728966
HLIrs794728966
Exacrs794728966
Varsomers794728966
Maprs794728966
PheGenIrs794728966
hapmaprs794728966
1000 genomesrs794728966
hgdprs794728966
ensemblrs794728966
gopubmedrs794728966
geneviewrs794728966
scholarrs794728966
googlers794728966
pharmgkbrs794728966
gwascentralrs794728966
openSNPrs794728966
23andMers794728966
23andMe allrs794728966
SNP Nexus

SNPshotrs794728966
SNPdbers794728966
MSV3drs794728966
GWAS Ctlgrs794728966
Max Magnitude0
ClinVar
Risk rs794728966(A;A)
Alt rs794728966(A;A)
Reference rs794728966(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ACTN2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.236925760G>A
CLNSRC
CLNACC RCV000183254.1,