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rs786205458

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786205458(A;A)
Make rs786205458(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position74589296
GeneADK
is asnp
is mentioned by
dbSNPrs786205458
ebirs786205458
HLIrs786205458
Exacrs786205458
Varsomers786205458
Maprs786205458
PheGenIrs786205458
hapmaprs786205458
1000 genomesrs786205458
hgdprs786205458
ensemblrs786205458
gopubmedrs786205458
geneviewrs786205458
scholarrs786205458
googlers786205458
pharmgkbrs786205458
gwascentralrs786205458
openSNPrs786205458
23andMers786205458
23andMe allrs786205458
SNP Nexus

SNPshotrs786205458
SNPdbers786205458
MSV3drs786205458
GWAS Ctlgrs786205458
Max Magnitude0
ClinVar
Risk rs786205458(A;A)
Alt rs786205458(A;A)
Reference rs786205458(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ADK
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.76349054T>A
CLNSRC
CLNACC RCV000171178.1,