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rs786205453

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786205453(A;G)
Make rs786205453(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position236720170
GeneACTN2
is asnp
is mentioned by
dbSNPrs786205453
ebirs786205453
HLIrs786205453
Exacrs786205453
Varsomers786205453
Maprs786205453
PheGenIrs786205453
hapmaprs786205453
1000 genomesrs786205453
hgdprs786205453
ensemblrs786205453
gopubmedrs786205453
geneviewrs786205453
scholarrs786205453
googlers786205453
pharmgkbrs786205453
gwascentralrs786205453
openSNPrs786205453
23andMers786205453
23andMe allrs786205453
SNP Nexus

SNPshotrs786205453
SNPdbers786205453
MSV3drs786205453
GWAS Ctlgrs786205453
Max Magnitude0
ClinVar
Risk rs786205453(G;G)
Alt rs786205453(G;G)
Reference rs786205453(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ACTN2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.236883470A>G
CLNSRC
CLNACC RCV000171170.1,