rs869025315

Orientation

plus

Stabilized

plus

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

Make rs869025315(C;T)

Make rs869025315(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

3

Position

66369505

Gene

SLC25A26

is a	snp
is	mentioned by
dbSNP	rs869025315
dbSNP (classic)	rs869025315
ClinGen	rs869025315
ebi	rs869025315
HLI	rs869025315
Exac	rs869025315
Gnomad	rs869025315
Varsome	rs869025315
LitVar	rs869025315
Map	rs869025315
PheGenI	rs869025315
Biobank	rs869025315
1000 genomes	rs869025315
hgdp	rs869025315
ensembl	rs869025315
geneview	rs869025315
scholar	rs869025315
google	rs869025315
pharmgkb	rs869025315
gwascentral	rs869025315
openSNP	rs869025315
23andMe	rs869025315
SNPshot	rs869025315
SNPdbe	rs869025315
MSV3d	rs869025315
GWAS Ctlg	rs869025315

Max Magnitude

0

ClinVar
Risk	rs869025315(T;T)
Alt	rs869025315(T;T)
Reference	Rs869025315(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.66419929C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000207463.1,