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rs188802138

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs188802138(C;T)
Make rs188802138(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position50528591
GeneTYMP
is asnp
is mentioned by
dbSNPrs188802138
ebirs188802138
HLIrs188802138
Exacrs188802138
Varsomers188802138
Maprs188802138
PheGenIrs188802138
hapmaprs188802138
1000 genomesrs188802138
hgdprs188802138
ensemblrs188802138
gopubmedrs188802138
geneviewrs188802138
scholarrs188802138
googlers188802138
pharmgkbrs188802138
gwascentralrs188802138
openSNPrs188802138
23andMers188802138
23andMe allrs188802138
SNP Nexus

SNPshotrs188802138
SNPdbers188802138
MSV3drs188802138
GWAS Ctlgrs188802138
Max Magnitude0
ClinVar
Risk rs188802138(T;T)
Alt rs188802138(T;T)
Reference rs188802138(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TYMP
CLNDBN not provided
Reversed 0
HGVS NC_000022.10:g.50967020C>T
CLNSRC
CLNACC RCV000198648.1,