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rs772909106

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs772909106(A;A)
Make rs772909106(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position236754026
GeneACTN2
is asnp
is mentioned by
dbSNPrs772909106
ebirs772909106
HLIrs772909106
Exacrs772909106
Varsomers772909106
Maprs772909106
PheGenIrs772909106
hapmaprs772909106
1000 genomesrs772909106
hgdprs772909106
ensemblrs772909106
gopubmedrs772909106
geneviewrs772909106
scholarrs772909106
googlers772909106
pharmgkbrs772909106
gwascentralrs772909106
openSNPrs772909106
23andMers772909106
23andMe allrs772909106
SNP Nexus

SNPshotrs772909106
SNPdbers772909106
MSV3drs772909106
GWAS Ctlgrs772909106
Max Magnitude0
ClinVar
Risk rs772909106(A;A)
Alt rs772909106(A;A)
Reference rs772909106(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ACTN2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.236917326G>A
CLNSRC
CLNACC RCV000183267.2,