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rs374777494

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs374777494(A;A)
Make rs374777494(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position66517858
GeneTK2
is asnp
is mentioned by
dbSNPrs374777494
ebirs374777494
HLIrs374777494
Exacrs374777494
Varsomers374777494
Maprs374777494
PheGenIrs374777494
hapmaprs374777494
1000 genomesrs374777494
hgdprs374777494
ensemblrs374777494
gopubmedrs374777494
geneviewrs374777494
scholarrs374777494
googlers374777494
pharmgkbrs374777494
gwascentralrs374777494
openSNPrs374777494
23andMers374777494
23andMe allrs374777494
SNP Nexus

SNPshotrs374777494
SNPdbers374777494
MSV3drs374777494
GWAS Ctlgrs374777494
Max Magnitude0
ClinVar
Risk rs374777494(A,T;A,T)
Alt rs374777494(A,T;A,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,