rs1064792864

Orientation

minus

Stabilized

minus

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

Chromosome

22

Position

50528550

Gene

TYMP

is a	snp
is	mentioned by
dbSNP	rs1064792864
dbSNP (classic)	rs1064792864
ClinGen	rs1064792864
ebi	rs1064792864
HLI	rs1064792864
Exac	rs1064792864
Gnomad	rs1064792864
Varsome	rs1064792864
LitVar	rs1064792864
Map	rs1064792864
PheGenI	rs1064792864
Biobank	rs1064792864
1000 genomes	rs1064792864
hgdp	rs1064792864
ensembl	rs1064792864
geneview	rs1064792864
scholar	rs1064792864
google	rs1064792864
pharmgkb	rs1064792864
gwascentral	rs1064792864
openSNP	rs1064792864
23andMe	rs1064792864
SNPshot	rs1064792864
SNPdbe	rs1064792864
MSV3d	rs1064792864
GWAS Ctlg	rs1064792864

Max Magnitude

0

ClinVar
Risk	rs1064792864(C;C)
Alt	rs1064792864(C;C)
Reference	Rs1064792864(T;T)
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.50966979A>G
CLNSRC
CLNACC	RCV000208643.1,