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rs863224250

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224250(A;A)
Make rs863224250(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position50529195
GeneTYMP
is asnp
is mentioned by
dbSNPrs863224250
ebirs863224250
HLIrs863224250
Exacrs863224250
Varsomers863224250
Maprs863224250
PheGenIrs863224250
hapmaprs863224250
1000 genomesrs863224250
hgdprs863224250
ensemblrs863224250
gopubmedrs863224250
geneviewrs863224250
scholarrs863224250
googlers863224250
pharmgkbrs863224250
gwascentralrs863224250
openSNPrs863224250
23andMers863224250
23andMe allrs863224250
SNP Nexus

SNPshotrs863224250
SNPdbers863224250
MSV3drs863224250
GWAS Ctlgrs863224250
Max Magnitude0
ClinVar
Risk rs863224250(A;A)
Alt rs863224250(A;A)
Reference rs863224250(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TYMP
CLNDBN not provided
Reversed 1
HGVS NC_000022.10:g.50967624C>T
CLNSRC
CLNACC RCV000198166.2,