rs797044878

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs797044878(A;A)

Make rs797044878(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

16

Position

56336763

Gene

GNAO1

is a	snp
is	mentioned by
dbSNP	rs797044878
dbSNP (classic)	rs797044878
ClinGen	rs797044878
ebi	rs797044878
HLI	rs797044878
Exac	rs797044878
Gnomad	rs797044878
Varsome	rs797044878
LitVar	rs797044878
Map	rs797044878
PheGenI	rs797044878
Biobank	rs797044878
1000 genomes	rs797044878
hgdp	rs797044878
ensembl	rs797044878
geneview	rs797044878
scholar	rs797044878
google	rs797044878
pharmgkb	rs797044878
gwascentral	rs797044878
openSNP	rs797044878
23andMe	rs797044878
SNPshot	rs797044878
SNPdbe	rs797044878
MSV3d	rs797044878
GWAS Ctlg	rs797044878

Max Magnitude

0

ClinVar
Risk	rs797044878(A;A)
Alt	rs797044878(A;A)
Reference	Rs797044878(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.56370675G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000190691.1, RCV000255659.2, RCV000490633.1,