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rs398124599

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs398124599(-;-)
Make rs398124599(-;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position80203145
GeneBCKDHB
is asnp
is mentioned by
dbSNPrs398124599
ebirs398124599
HLIrs398124599
Exacrs398124599
Varsomers398124599
Maprs398124599
PheGenIrs398124599
hapmaprs398124599
1000 genomesrs398124599
hgdprs398124599
ensemblrs398124599
gopubmedrs398124599
geneviewrs398124599
scholarrs398124599
googlers398124599
pharmgkbrs398124599
gwascentralrs398124599
openSNPrs398124599
23andMers398124599
23andMe allrs398124599
SNP Nexus

SNPshotrs398124599
SNPdbers398124599
MSV3drs398124599
GWAS Ctlgrs398124599
Max Magnitude0
ClinVar
Risk rs398124599(;)
Alt rs398124599(;)
Reference rs398124599(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene BCKDHB
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.80912862delT
CLNSRC ClinVar
CLNACC RCV000082776.3,