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rs138867882

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs138867882(A;A)
Make rs138867882(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position47580977
GeneKBTBD4, NDUFS3
is asnp
is mentioned by
dbSNPrs138867882
dbSNP (classic)rs138867882
ClinGenrs138867882
ebirs138867882
HLIrs138867882
Exacrs138867882
Gnomadrs138867882
Varsomers138867882
LitVarrs138867882
Maprs138867882
PheGenIrs138867882
Biobankrs138867882
1000 genomesrs138867882
hgdprs138867882
ensemblrs138867882
geneviewrs138867882
scholarrs138867882
googlers138867882
pharmgkbrs138867882
gwascentralrs138867882
openSNPrs138867882
23andMers138867882
SNPshotrs138867882
SNPdbers138867882
MSV3drs138867882
GWAS Ctlgrs138867882
Max Magnitude0
ClinVar
Risk rs138867882(A;A)
Alt rs138867882(A;A)
Reference Rs138867882(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NDUFS3 KBTBD4
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.47602529G>A
CLNSRC
CLNACC RCV000479127.1,