rs1064792889

Orientation

minus

Stabilized

minus

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

Chromosome

22

Position

50525908

Gene	SCO2, TYMP

is a	snp
is	mentioned by
dbSNP	rs1064792889
dbSNP (classic)	rs1064792889
ClinGen	rs1064792889
ebi	rs1064792889
HLI	rs1064792889
Exac	rs1064792889
Gnomad	rs1064792889
Varsome	rs1064792889
LitVar	rs1064792889
Map	rs1064792889
PheGenI	rs1064792889
Biobank	rs1064792889
1000 genomes	rs1064792889
hgdp	rs1064792889
ensembl	rs1064792889
geneview	rs1064792889
scholar	rs1064792889
google	rs1064792889
pharmgkb	rs1064792889
gwascentral	rs1064792889
openSNP	rs1064792889
23andMe	rs1064792889
SNPshot	rs1064792889
SNPdbe	rs1064792889
MSV3d	rs1064792889
GWAS Ctlg	rs1064792889

Max Magnitude

0

ClinVar
Risk	rs1064792889(-;-)
Alt	rs1064792889(-;-)
Reference	Rs1064792889(G;G)
Significance	Pathogenic
Disease	Mitochondrial DNA depletion syndrome 1 (MNGIE type)
Variation	info
Gene	TYMP SCO2
CLNDBN	Mitochondrial DNA depletion syndrome 1 (MNGIE type)
Reversed	1
HGVS	NC_000022.10:g.50964337delC
CLNSRC
CLNACC	RCV000208678.1,