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rs864321624

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs864321624(A;G)
Make rs864321624(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position19110790
GeneSLC25A42
is asnp
is mentioned by
dbSNPrs864321624
ebirs864321624
HLIrs864321624
Exacrs864321624
Varsomers864321624
Maprs864321624
PheGenIrs864321624
hapmaprs864321624
1000 genomesrs864321624
hgdprs864321624
ensemblrs864321624
gopubmedrs864321624
geneviewrs864321624
scholarrs864321624
googlers864321624
pharmgkbrs864321624
gwascentralrs864321624
openSNPrs864321624
23andMers864321624
23andMe allrs864321624
SNP Nexus

SNPshotrs864321624
SNPdbers864321624
MSV3drs864321624
GWAS Ctlgrs864321624
Max Magnitude0
ClinVar
Risk rs864321624(G;G)
Alt rs864321624(G;G)
Reference rs864321624(A;A)
Significance Probable-Pathogenic
Disease Mitochondrial myopathy
Variation info
Gene SLC25A42
CLNDBN Mitochondrial myopathy
Reversed 0
HGVS NC_000019.9:g.19221599A>G
CLNSRC
CLNACC RCV000203566.1,