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rs863224254

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224254(A;A)
Make rs863224254(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position50526082
GeneSCO2, TYMP
is asnp
is mentioned by
dbSNPrs863224254
ebirs863224254
HLIrs863224254
Exacrs863224254
Varsomers863224254
Maprs863224254
PheGenIrs863224254
hapmaprs863224254
1000 genomesrs863224254
hgdprs863224254
ensemblrs863224254
gopubmedrs863224254
geneviewrs863224254
scholarrs863224254
googlers863224254
pharmgkbrs863224254
gwascentralrs863224254
openSNPrs863224254
23andMers863224254
23andMe allrs863224254
SNP Nexus

SNPshotrs863224254
SNPdbers863224254
MSV3drs863224254
GWAS Ctlgrs863224254
Max Magnitude0
ClinVar
Risk rs863224254(A,C;A,C)
Alt rs863224254(A,C;A,C)
Reference rs863224254(G;G)
Significance Probable-Pathogenic
Disease not specified not provided
Variation info
Gene TYMP SCO2
CLNDBN not specified not provided
Reversed 1
HGVS NC_000022.10:g.50964511C>G; NC_000022.10:g.50964511C>T
CLNSRC
CLNACC RCV000197532.1, RCV000196011.1,