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rs797044951

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797044951(A;A)
Make rs797044951(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position56351396
GeneGNAO1
is asnp
is mentioned by
dbSNPrs797044951
dbSNP (old)rs797044951
ClinGenrs797044951
ebirs797044951
HLIrs797044951
Exacrs797044951
Gnomadrs797044951
Varsomers797044951
Maprs797044951
PheGenIrs797044951
Biobankrs797044951
1000 genomesrs797044951
hgdprs797044951
ensemblrs797044951
gopubmedrs797044951
geneviewrs797044951
scholarrs797044951
googlers797044951
pharmgkbrs797044951
gwascentralrs797044951
openSNPrs797044951
23andMers797044951
23andMe allrs797044951
SNP Nexus

SNPshotrs797044951
SNPdbers797044951
MSV3drs797044951
GWAS Ctlgrs797044951
Max Magnitude0
ClinVar
Risk rs797044951(A;A)
Alt rs797044951(A;A)
Reference Rs797044951(G;G)
Significance Pathogenic
Disease Inborn genetic diseases not provided Neurodevelopmental disorder with involuntary movements
Variation info
Gene GNAO1
CLNDBN Inborn genetic diseases not provided Neurodevelopmental disorder with involuntary movements
Reversed 0
HGVS NC_000016.9:g.56385308G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000190803.1, RCV000254701.1, RCV000490631.1,