rs1064792860

Orientation

minus

Stabilized

minus

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

Chromosome

22

Position

50529225

Gene

TYMP

is a	snp
is	mentioned by
dbSNP	rs1064792860
dbSNP (classic)	rs1064792860
ClinGen	rs1064792860
ebi	rs1064792860
HLI	rs1064792860
Exac	rs1064792860
Gnomad	rs1064792860
Varsome	rs1064792860
LitVar	rs1064792860
Map	rs1064792860
PheGenI	rs1064792860
Biobank	rs1064792860
1000 genomes	rs1064792860
hgdp	rs1064792860
ensembl	rs1064792860
geneview	rs1064792860
scholar	rs1064792860
google	rs1064792860
pharmgkb	rs1064792860
gwascentral	rs1064792860
openSNP	rs1064792860
23andMe	rs1064792860
SNPshot	rs1064792860
SNPdbe	rs1064792860
MSV3d	rs1064792860
GWAS Ctlg	rs1064792860

Max Magnitude

0

ClinVar
Risk	rs1064792860(T;T)
Alt	rs1064792860(T;T)
Reference	Rs1064792860(C;C)
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.50967654G>A
CLNSRC
CLNACC	RCV000208694.1,