Have questions? Visit https://www.reddit.com/r/SNPedia

rs773888308

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs773888308(A;A)
Make rs773888308(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position49738249
GeneOGDHL
is asnp
is mentioned by
dbSNPrs773888308
dbSNP (classic)rs773888308
ClinGenrs773888308
ebirs773888308
HLIrs773888308
Exacrs773888308
Gnomadrs773888308
Varsomers773888308
LitVarrs773888308
Maprs773888308
PheGenIrs773888308
Biobankrs773888308
1000 genomesrs773888308
hgdprs773888308
ensemblrs773888308
geneviewrs773888308
scholarrs773888308
googlers773888308
pharmgkbrs773888308
gwascentralrs773888308
openSNPrs773888308
23andMers773888308
SNPshotrs773888308
SNPdbers773888308
MSV3drs773888308
GWAS Ctlgrs773888308
Max Magnitude0
ClinVar
Risk rs773888308(A;A)
Alt rs773888308(A;A)
Reference Rs773888308(G;G)
Significance Probable-Pathogenic
Disease Abnormality of brain morphology
Variation info
Gene OGDHL
CLNDBN Abnormality of brain morphology
Reversed 0
HGVS NC_000010.10:g.50946295G>A
CLNSRC
CLNACC RCV000454186.1,