rs1064792885

Orientation

minus

Stabilized

minus

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

Chromosome

22

Position

50525787

Gene	SCO2, TYMP

is a	snp
is	mentioned by
dbSNP	rs1064792885
dbSNP (classic)	rs1064792885
ClinGen	rs1064792885
ebi	rs1064792885
HLI	rs1064792885
Exac	rs1064792885
Gnomad	rs1064792885
Varsome	rs1064792885
LitVar	rs1064792885
Map	rs1064792885
PheGenI	rs1064792885
Biobank	rs1064792885
1000 genomes	rs1064792885
hgdp	rs1064792885
ensembl	rs1064792885
geneview	rs1064792885
scholar	rs1064792885
google	rs1064792885
pharmgkb	rs1064792885
gwascentral	rs1064792885
openSNP	rs1064792885
23andMe	rs1064792885
SNPshot	rs1064792885
SNPdbe	rs1064792885
MSV3d	rs1064792885
GWAS Ctlg	rs1064792885

Max Magnitude

0

ClinVar
Risk	rs1064792885(T;T)
Alt	rs1064792885(T;T)
Reference	Rs1064792885(-;-)
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.50964217dup
CLNSRC
CLNACC	RCV000208688.1,