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rs878853051

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs878853051(A;G)
Make rs878853051(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position56354971
GeneGNAO1
is asnp
is mentioned by
dbSNPrs878853051
ebirs878853051
HLIrs878853051
Exacrs878853051
Varsomers878853051
Maprs878853051
PheGenIrs878853051
hapmaprs878853051
1000 genomesrs878853051
hgdprs878853051
ensemblrs878853051
gopubmedrs878853051
geneviewrs878853051
scholarrs878853051
googlers878853051
pharmgkbrs878853051
gwascentralrs878853051
openSNPrs878853051
23andMers878853051
23andMe allrs878853051
SNP Nexus

SNPshotrs878853051
SNPdbers878853051
MSV3drs878853051
GWAS Ctlgrs878853051
Max Magnitude0
ClinVar
Risk rs878853051(G;G)
Alt rs878853051(G;G)
Reference rs878853051(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GNAO1
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.56388883A>G
CLNSRC
CLNACC RCV000224477.1,