rs374777494

Orientation

plus

Stabilized

plus

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

Make rs374777494(A;A)

Make rs374777494(A;C)

Reference

GRCh38.p2 38.2/146

Chromosome

16

Position

66517858

Gene

TK2

is a	snp
is	mentioned by
dbSNP	rs374777494
dbSNP (classic)	rs374777494
ClinGen	rs374777494
ebi	rs374777494
HLI	rs374777494
Exac	rs374777494
Gnomad	rs374777494
Varsome	rs374777494
LitVar	rs374777494
Map	rs374777494
PheGenI	rs374777494
Biobank	rs374777494
1000 genomes	rs374777494
hgdp	rs374777494
ensembl	rs374777494
geneview	rs374777494
scholar	rs374777494
google	rs374777494
pharmgkb	rs374777494
gwascentral	rs374777494
openSNP	rs374777494
23andMe	rs374777494
SNPshot	rs374777494
SNPdbe	rs374777494
MSV3d	rs374777494
GWAS Ctlg	rs374777494

Max Magnitude

0

ClinVar
Risk	rs374777494(A;A) rs374777494(T;T)
Alt	rs374777494(A;A) rs374777494(T;T)
Reference	Rs374777494(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	TK2
CLNDBN	not provided
Reversed	0
HGVS	NC_000016.9:g.66551761C>T
CLNSRC
CLNACC	RCV000199938.2,