rs1064792859

Orientation

minus

Stabilized

minus

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

Chromosome

22

Position

50529325

Gene

TYMP

is a	snp
is	mentioned by
dbSNP	rs1064792859
dbSNP (classic)	rs1064792859
ClinGen	rs1064792859
ebi	rs1064792859
HLI	rs1064792859
Exac	rs1064792859
Gnomad	rs1064792859
Varsome	rs1064792859
LitVar	rs1064792859
Map	rs1064792859
PheGenI	rs1064792859
Biobank	rs1064792859
1000 genomes	rs1064792859
hgdp	rs1064792859
ensembl	rs1064792859
geneview	rs1064792859
scholar	rs1064792859
google	rs1064792859
pharmgkb	rs1064792859
gwascentral	rs1064792859
openSNP	rs1064792859
23andMe	rs1064792859
SNPshot	rs1064792859
SNPdbe	rs1064792859
MSV3d	rs1064792859
GWAS Ctlg	rs1064792859

Max Magnitude

0

ClinVar
Risk	rs1064792859(A;A)
Alt	rs1064792859(A;A)
Reference	Rs1064792859(G;G)
Significance	Pathogenic
Disease	Mitochondrial DNA depletion syndrome 1 (MNGIE type)
Variation	info
Gene	TYMP
CLNDBN	Mitochondrial DNA depletion syndrome 1 (MNGIE type)
Reversed	1
HGVS	NC_000022.10:g.50967754C>T
CLNSRC
CLNACC	RCV000208657.1,