Have questions? Visit https://www.reddit.com/r/SNPedia

rs794728960

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728960(A;A)
Make rs794728960(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position236719005
GeneACTN2
is asnp
is mentioned by
dbSNPrs794728960
ebirs794728960
HLIrs794728960
Exacrs794728960
Varsomers794728960
Maprs794728960
PheGenIrs794728960
hapmaprs794728960
1000 genomesrs794728960
hgdprs794728960
ensemblrs794728960
gopubmedrs794728960
geneviewrs794728960
scholarrs794728960
googlers794728960
pharmgkbrs794728960
gwascentralrs794728960
openSNPrs794728960
23andMers794728960
23andMe allrs794728960
SNP Nexus

SNPshotrs794728960
SNPdbers794728960
MSV3drs794728960
GWAS Ctlgrs794728960
Max Magnitude0
ClinVar
Risk rs794728960(A;A)
Alt rs794728960(A;A)
Reference rs794728960(G;G)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene ACTN2
CLNDBN not specified
Reversed 0
HGVS NC_000001.10:g.236882305G>A
CLNSRC
CLNACC RCV000183247.2,