rs138479499

Orientation

plus

Stabilized

plus

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

Make rs138479499(C;T)

Make rs138479499(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

16

Position

66529028

Gene

TK2

is a	snp
is	mentioned by
dbSNP	rs138479499
dbSNP (classic)	rs138479499
ClinGen	rs138479499
ebi	rs138479499
HLI	rs138479499
Exac	rs138479499
Gnomad	rs138479499
Varsome	rs138479499
LitVar	rs138479499
Map	rs138479499
PheGenI	rs138479499
Biobank	rs138479499
1000 genomes	rs138479499
hgdp	rs138479499
ensembl	rs138479499
geneview	rs138479499
scholar	rs138479499
google	rs138479499
pharmgkb	rs138479499
gwascentral	rs138479499
openSNP	rs138479499
23andMe	rs138479499
SNPshot	rs138479499
SNPdbe	rs138479499
MSV3d	rs138479499
GWAS Ctlg	rs138479499

Max Magnitude

0

ClinVar
Risk	rs138479499(T;T)
Alt	rs138479499(T;T)
Reference	Rs138479499(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	TK2
CLNDBN	not provided
Reversed	0
HGVS	NC_000016.9:g.66562931C>T
CLNSRC
CLNACC	RCV000198744.1,