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rs112384084

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs112384084(C;T)
Make rs112384084(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position195867623
GeneTNK2
is asnp
is mentioned by
dbSNPrs112384084
ebirs112384084
HLIrs112384084
Exacrs112384084
Varsomers112384084
Maprs112384084
PheGenIrs112384084
hapmaprs112384084
1000 genomesrs112384084
hgdprs112384084
ensemblrs112384084
gopubmedrs112384084
geneviewrs112384084
scholarrs112384084
googlers112384084
pharmgkbrs112384084
gwascentralrs112384084
openSNPrs112384084
23andMers112384084
23andMe allrs112384084
SNP Nexus

SNPshotrs112384084
SNPdbers112384084
MSV3drs112384084
GWAS Ctlgrs112384084
Max Magnitude0
ClinVar
Risk rs112384084(T;T)
Alt rs112384084(T;T)
Reference rs112384084(C;C)
Significance Probable-Pathogenic
Disease Parkinson disease
Variation info
Gene TNK2
CLNDBN Parkinson disease
Reversed 0
HGVS NC_000003.11:g.195594494C>T
CLNSRC
CLNACC RCV000210436.1,