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rs797044878

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797044878(A;A)
Make rs797044878(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position56336763
GeneGNAO1
is asnp
is mentioned by
dbSNPrs797044878
ebirs797044878
HLIrs797044878
Exacrs797044878
Varsomers797044878
Maprs797044878
PheGenIrs797044878
hapmaprs797044878
1000 genomesrs797044878
hgdprs797044878
ensemblrs797044878
gopubmedrs797044878
geneviewrs797044878
scholarrs797044878
googlers797044878
pharmgkbrs797044878
gwascentralrs797044878
openSNPrs797044878
23andMers797044878
23andMe allrs797044878
SNP Nexus

SNPshotrs797044878
SNPdbers797044878
MSV3drs797044878
GWAS Ctlgrs797044878
Max Magnitude0
ClinVar
Risk rs797044878(A;A)
Alt rs797044878(A;A)
Reference rs797044878(G;G)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene GNAO1
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000016.9:g.56370675G>A
CLNSRC
CLNACC RCV000190691.1,