rs869025314

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs869025314(C;T)

Make rs869025314(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

3

Position

66262055

Gene

SLC25A26

is a	snp
is	mentioned by
dbSNP	rs869025314
dbSNP (classic)	rs869025314
ClinGen	rs869025314
ebi	rs869025314
HLI	rs869025314
Exac	rs869025314
Gnomad	rs869025314
Varsome	rs869025314
LitVar	rs869025314
Map	rs869025314
PheGenI	rs869025314
Biobank	rs869025314
1000 genomes	rs869025314
hgdp	rs869025314
ensembl	rs869025314
geneview	rs869025314
scholar	rs869025314
google	rs869025314
pharmgkb	rs869025314
gwascentral	rs869025314
openSNP	rs869025314
23andMe	rs869025314
SNPshot	rs869025314
SNPdbe	rs869025314
MSV3d	rs869025314
GWAS Ctlg	rs869025314

Max Magnitude

0

ClinVar
Risk	rs869025314(T;T)
Alt	rs869025314(T;T)
Reference	Rs869025314(C;C)
Significance	Pathogenic
Disease	Combined oxidative phosphorylation deficiency 28
Variation	info
Gene	SLC25A26
CLNDBN	Combined oxidative phosphorylation deficiency 28
Reversed	0
HGVS	NC_000003.11:g.66312479C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000207457.1,