rs28359178

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0

Make rs28359178(A;A)

Make rs28359178(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

13708

Gene

ND5

is a	snp
is	mentioned by
dbSNP	rs28359178
dbSNP (classic)	rs28359178
ClinGen	rs28359178
ebi	rs28359178
HLI	rs28359178
Exac	rs28359178
Gnomad	rs28359178
Varsome	rs28359178
LitVar	rs28359178
Map	rs28359178
PheGenI	rs28359178
Biobank	rs28359178
1000 genomes	rs28359178
hgdp	rs28359178
ensembl	rs28359178
geneview	rs28359178
scholar	rs28359178
google	rs28359178
pharmgkb	rs28359178
gwascentral	rs28359178
openSNP	rs28359178
23andMe	rs28359178
SNPshot	rs28359178
SNPdbe	rs28359178
MSV3d	rs28359178
GWAS Ctlg	rs28359178

GMAF

0.07103

Max Magnitude

0

?	(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,