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rs748559929

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs748559929(C;T)
Make rs748559929(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position50526241
GeneSCO2, TYMP
is asnp
is mentioned by
dbSNPrs748559929
ebirs748559929
HLIrs748559929
Exacrs748559929
Varsomers748559929
Maprs748559929
PheGenIrs748559929
hapmaprs748559929
1000 genomesrs748559929
hgdprs748559929
ensemblrs748559929
gopubmedrs748559929
geneviewrs748559929
scholarrs748559929
googlers748559929
pharmgkbrs748559929
gwascentralrs748559929
openSNPrs748559929
23andMers748559929
23andMe allrs748559929
SNP Nexus

SNPshotrs748559929
SNPdbers748559929
MSV3drs748559929
GWAS Ctlgrs748559929
Max Magnitude0
ClinVar
Risk rs748559929(G;G)
Alt rs748559929(G;G)
Reference rs748559929(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TYMP SCO2
CLNDBN not provided
Reversed 0
HGVS NC_000022.10:g.50964670C>T
CLNSRC
CLNACC RCV000196301.2,