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rs587777055

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587777055(A;G)
Make rs587777055(G;G)
ReferenceGRCh38 38.1/142
Chromosome16
Position56334785
GeneGNAO1
is asnp
is mentioned by
dbSNPrs587777055
ebirs587777055
HLIrs587777055
Exacrs587777055
Varsomers587777055
Maprs587777055
PheGenIrs587777055
hapmaprs587777055
1000 genomesrs587777055
hgdprs587777055
ensemblrs587777055
gopubmedrs587777055
geneviewrs587777055
scholarrs587777055
googlers587777055
pharmgkbrs587777055
gwascentralrs587777055
openSNPrs587777055
23andMers587777055
23andMe allrs587777055
SNP Nexus

SNPshotrs587777055
SNPdbers587777055
MSV3drs587777055
GWAS Ctlgrs587777055
Max Magnitude0
ClinVar
Risk rs587777055(G;G)
Alt rs587777055(G;G)
Reference rs587777055(A;A)
Significance Pathogenic
Disease Early infantile epileptic encephalopathy 17
Variation info
Gene GNAO1
CLNDBN Early infantile epileptic encephalopathy 17
Reversed 0
HGVS NC_000016.9:g.56368697A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000056406.26,