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rs138479499

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs138479499(C;T)
Make rs138479499(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position66529028
GeneTK2
is asnp
is mentioned by
dbSNPrs138479499
ebirs138479499
HLIrs138479499
Exacrs138479499
Varsomers138479499
Maprs138479499
PheGenIrs138479499
hapmaprs138479499
1000 genomesrs138479499
hgdprs138479499
ensemblrs138479499
gopubmedrs138479499
geneviewrs138479499
scholarrs138479499
googlers138479499
pharmgkbrs138479499
gwascentralrs138479499
openSNPrs138479499
23andMers138479499
23andMe allrs138479499
SNP Nexus

SNPshotrs138479499
SNPdbers138479499
MSV3drs138479499
GWAS Ctlgrs138479499
Max Magnitude0
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,