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rs863224251

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863224251(A;T)
Make rs863224251(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position50528552
GeneTYMP
is asnp
is mentioned by
dbSNPrs863224251
ebirs863224251
HLIrs863224251
Exacrs863224251
Varsomers863224251
Maprs863224251
PheGenIrs863224251
hapmaprs863224251
1000 genomesrs863224251
hgdprs863224251
ensemblrs863224251
gopubmedrs863224251
geneviewrs863224251
scholarrs863224251
googlers863224251
pharmgkbrs863224251
gwascentralrs863224251
openSNPrs863224251
23andMers863224251
23andMe allrs863224251
SNP Nexus

SNPshotrs863224251
SNPdbers863224251
MSV3drs863224251
GWAS Ctlgrs863224251
Max Magnitude0
ClinVar
Risk rs863224251(T;T)
Alt rs863224251(T;T)
Reference rs863224251(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TYMP
CLNDBN not provided
Reversed 1
HGVS NC_000022.10:g.50966981T>A
CLNSRC
CLNACC RCV000200518.1,