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rs752513525

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs752513525(A;A)
Make rs752513525(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position19526257
GeneNDUFA13
is asnp
is mentioned by
dbSNPrs752513525
ebirs752513525
HLIrs752513525
Exacrs752513525
Varsomers752513525
Maprs752513525
PheGenIrs752513525
hapmaprs752513525
1000 genomesrs752513525
hgdprs752513525
ensemblrs752513525
gopubmedrs752513525
geneviewrs752513525
scholarrs752513525
googlers752513525
pharmgkbrs752513525
gwascentralrs752513525
openSNPrs752513525
23andMers752513525
23andMe allrs752513525
SNP Nexus

SNPshotrs752513525
SNPdbers752513525
MSV3drs752513525
GWAS Ctlgrs752513525
Max Magnitude0
ClinVar
Risk rs752513525(A;A)
Alt rs752513525(A;A)
Reference rs752513525(G;G)
Significance Pathogenic
Disease Mitochondrial complex I deficiency
Variation info
Gene NDUFA13
CLNDBN Mitochondrial complex I deficiency
Reversed 0
HGVS NC_000019.9:g.19637066G>A
CLNSRC
CLNACC RCV000239442.1,