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rs863224255

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863224255(A;A)
Make rs863224255(A;C)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position50529162
GeneTYMP
is asnp
is mentioned by
dbSNPrs863224255
ebirs863224255
HLIrs863224255
Exacrs863224255
Varsomers863224255
Maprs863224255
PheGenIrs863224255
hapmaprs863224255
1000 genomesrs863224255
hgdprs863224255
ensemblrs863224255
gopubmedrs863224255
geneviewrs863224255
scholarrs863224255
googlers863224255
pharmgkbrs863224255
gwascentralrs863224255
openSNPrs863224255
23andMers863224255
23andMe allrs863224255
SNP Nexus

SNPshotrs863224255
SNPdbers863224255
MSV3drs863224255
GWAS Ctlgrs863224255
Max Magnitude0
ClinVar
Risk rs863224255(A;A)
Alt rs863224255(A;A)
Reference rs863224255(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TYMP
CLNDBN not provided
Reversed 1
HGVS NC_000022.10:g.50967591G>T
CLNSRC
CLNACC RCV000195809.1,