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rs761389904

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs761389904(G;G)
Make rs761389904(G;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position13816520
GeneNDUFAF5
is asnp
is mentioned by
dbSNPrs761389904
ebirs761389904
HLIrs761389904
Exacrs761389904
Varsomers761389904
Maprs761389904
PheGenIrs761389904
hapmaprs761389904
1000 genomesrs761389904
hgdprs761389904
ensemblrs761389904
gopubmedrs761389904
geneviewrs761389904
scholarrs761389904
googlers761389904
pharmgkbrs761389904
gwascentralrs761389904
openSNPrs761389904
23andMers761389904
23andMe allrs761389904
SNP Nexus

SNPshotrs761389904
SNPdbers761389904
MSV3drs761389904
GWAS Ctlgrs761389904
Max Magnitude0
ClinVar
Risk rs761389904(G;G)
Alt rs761389904(G;G)
Reference rs761389904(T;T)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene NDUFAF5
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000020.10:g.13797166T>G
CLNSRC
CLNACC RCV000210569.1,