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rs746405080

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs746405080(A;A)
Make rs746405080(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position13788614
GeneLOC105372540, NDUFAF5
is asnp
is mentioned by
dbSNPrs746405080
ebirs746405080
HLIrs746405080
Exacrs746405080
Varsomers746405080
Maprs746405080
PheGenIrs746405080
hapmaprs746405080
1000 genomesrs746405080
hgdprs746405080
ensemblrs746405080
gopubmedrs746405080
geneviewrs746405080
scholarrs746405080
googlers746405080
pharmgkbrs746405080
gwascentralrs746405080
openSNPrs746405080
23andMers746405080
23andMe allrs746405080
SNP Nexus

SNPshotrs746405080
SNPdbers746405080
MSV3drs746405080
GWAS Ctlgrs746405080
Max Magnitude0
ClinVar
Risk rs746405080(A;A)
Alt rs746405080(A;A)
Reference rs746405080(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NDUFAF5
CLNDBN not provided
Reversed 0
HGVS NC_000020.10:g.13769260G>A
CLNSRC
CLNACC RCV000197446.1,