rs747276038

Orientation

plus

Stabilized

plus

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

Make rs747276038(C;C)

Make rs747276038(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

16

Position

66541929

Gene

TK2

is a	snp
is	mentioned by
dbSNP	rs747276038
dbSNP (classic)	rs747276038
ClinGen	rs747276038
ebi	rs747276038
HLI	rs747276038
Exac	rs747276038
Gnomad	rs747276038
Varsome	rs747276038
LitVar	rs747276038
Map	rs747276038
PheGenI	rs747276038
Biobank	rs747276038
1000 genomes	rs747276038
hgdp	rs747276038
ensembl	rs747276038
geneview	rs747276038
scholar	rs747276038
google	rs747276038
pharmgkb	rs747276038
gwascentral	rs747276038
openSNP	rs747276038
23andMe	rs747276038
SNPshot	rs747276038
SNPdbe	rs747276038
MSV3d	rs747276038
GWAS Ctlg	rs747276038

Max Magnitude

0

ClinVar
Risk	rs747276038(C;C)
Alt	rs747276038(C;C)
Reference	Rs747276038(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	TK2
CLNDBN	not provided
Reversed	0
HGVS	NC_000016.9:g.66575832T>C
CLNSRC
CLNACC	RCV000478863.1,