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rs142329098

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs142329098(C;T)
Make rs142329098(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome8
Position103403276
GeneSLC25A32
is asnp
is mentioned by
dbSNPrs142329098
ebirs142329098
HLIrs142329098
Exacrs142329098
Varsomers142329098
Maprs142329098
PheGenIrs142329098
hapmaprs142329098
1000 genomesrs142329098
hgdprs142329098
ensemblrs142329098
gopubmedrs142329098
geneviewrs142329098
scholarrs142329098
googlers142329098
pharmgkbrs142329098
gwascentralrs142329098
openSNPrs142329098
23andMers142329098
23andMe allrs142329098
SNP Nexus

SNPshotrs142329098
SNPdbers142329098
MSV3drs142329098
GWAS Ctlgrs142329098
Max Magnitude0
ClinVar
Risk rs142329098(T;T)
Alt rs142329098(T;T)
Reference rs142329098(C;C)
Significance Pathogenic
Disease Exercise intolerance
Variation info
Gene SLC25A32
CLNDBN Exercise intolerance, riboflavin-responsive
Reversed 0
HGVS NC_000008.10:g.104415504C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000208727.2,