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rs863224252

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863224252(A;A)
Make rs863224252(A;C)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position50526609
GeneSCO2, TYMP
is asnp
is mentioned by
dbSNPrs863224252
ebirs863224252
HLIrs863224252
Exacrs863224252
Varsomers863224252
Maprs863224252
PheGenIrs863224252
hapmaprs863224252
1000 genomesrs863224252
hgdprs863224252
ensemblrs863224252
gopubmedrs863224252
geneviewrs863224252
scholarrs863224252
googlers863224252
pharmgkbrs863224252
gwascentralrs863224252
openSNPrs863224252
23andMers863224252
23andMe allrs863224252
SNP Nexus

SNPshotrs863224252
SNPdbers863224252
MSV3drs863224252
GWAS Ctlgrs863224252
Max Magnitude0
ClinVar
Risk rs863224252(A;A)
Alt rs863224252(A;A)
Reference rs863224252(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TYMP SCO2
CLNDBN not provided
Reversed 1
HGVS NC_000022.10:g.50965038G>T
CLNSRC
CLNACC RCV000197047.1,