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rs367823977

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs367823977(A;G)
Make rs367823977(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position41422353
GeneBCKDHA
is asnp
is mentioned by
dbSNPrs367823977
ebirs367823977
HLIrs367823977
Exacrs367823977
Varsomers367823977
Maprs367823977
PheGenIrs367823977
hapmaprs367823977
1000 genomesrs367823977
hgdprs367823977
ensemblrs367823977
gopubmedrs367823977
geneviewrs367823977
scholarrs367823977
googlers367823977
pharmgkbrs367823977
gwascentralrs367823977
openSNPrs367823977
23andMers367823977
23andMe allrs367823977
SNP Nexus

SNPshotrs367823977
SNPdbers367823977
MSV3drs367823977
GWAS Ctlgrs367823977
Max Magnitude0
ClinVar
Risk rs367823977(G;G)
Alt rs367823977(G;G)
Reference rs367823977(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene BCKDHA
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.41928258A>G
CLNSRC
CLNACC RCV000224751.1,