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rs28359178

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0
Make rs28359178(A;A)
Make rs28359178(A;G)
ReferenceGRCh37.p10 37.5/138
ChromosomeMT
Position13708
GeneMT-ND5
is asnp
is mentioned by
dbSNPrs28359178
ebirs28359178
HLIrs28359178
Exacrs28359178
Varsomers28359178
Maprs28359178
PheGenIrs28359178
hapmaprs28359178
1000 genomesrs28359178
hgdprs28359178
ensemblrs28359178
gopubmedrs28359178
geneviewrs28359178
scholarrs28359178
googlers28359178
pharmgkbrs28359178
gwascentralrs28359178
openSNPrs28359178
23andMers28359178
23andMe allrs28359178
SNP Nexus

SNPshotrs28359178
SNPdbers28359178
MSV3drs28359178
GWAS Ctlgrs28359178
GMAF0.07103
Max Magnitude0
? (A;A) (A;G) (G;G) 28

[PMID 19387457] Association of UCP2 -866 G/A polymorphism with chronic inflammatory diseases


Haplogroup SNP
Alt. Name(s) G13708A
Source(s) None specified
Tree PhyloTree build 16
Clade
Haplogroup
No Clade Haplogroup
Ancestral
Haplogroup
Haplogroup H2a (mtDNA)
Derived
Haplogroup
Haplogroup H2a5 (mtDNA)
Ancestral Allele G
Derived Allele A



ClinVar
Risk rs28359178(A;A)
Alt rs28359178(A;A)
Reference rs28359178(G;G)
Significance Other
Disease Leber's optic atrophy
Variation info
Gene ND5
CLNDBN Leber's optic atrophy
Reversed 0
HGVS NC_012920.1:m.13708G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010336.4,