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rs146837138

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs146837138(A;A)
Make rs146837138(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position13785246
GeneESF1, NDUFAF5
is asnp
is mentioned by
dbSNPrs146837138
ebirs146837138
HLIrs146837138
Exacrs146837138
Varsomers146837138
Maprs146837138
PheGenIrs146837138
hapmaprs146837138
1000 genomesrs146837138
hgdprs146837138
ensemblrs146837138
gopubmedrs146837138
geneviewrs146837138
scholarrs146837138
googlers146837138
pharmgkbrs146837138
gwascentralrs146837138
openSNPrs146837138
23andMers146837138
23andMe allrs146837138
SNP Nexus

SNPshotrs146837138
SNPdbers146837138
MSV3drs146837138
GWAS Ctlgrs146837138
Max Magnitude0
ClinVar
Risk rs146837138(A;A)
Alt rs146837138(A;A)
Reference rs146837138(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NDUFAF5 ESF1
CLNDBN not provided
Reversed 0
HGVS NC_000020.10:g.13765892G>A
CLNSRC
CLNACC RCV000197548.1,