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rs786205559

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205559(A;A)
Make rs786205559(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome22
Position50529198
GeneTYMP
is asnp
is mentioned by
dbSNPrs786205559
ClinGenrs786205559
ebirs786205559
HLIrs786205559
Exacrs786205559
Varsomers786205559
Maprs786205559
PheGenIrs786205559
hapmaprs786205559
1000 genomesrs786205559
hgdprs786205559
ensemblrs786205559
gopubmedrs786205559
geneviewrs786205559
scholarrs786205559
googlers786205559
pharmgkbrs786205559
gwascentralrs786205559
openSNPrs786205559
23andMers786205559
23andMe allrs786205559
SNP Nexus

SNPshotrs786205559
SNPdbers786205559
MSV3drs786205559
GWAS Ctlgrs786205559
Max Magnitude0
ClinVar
Risk rs786205559(A;A)
Alt rs786205559(A;A)
Reference Rs786205559(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TYMP
CLNDBN not provided
Reversed 1
HGVS NC_000022.10:g.50967627C>T
CLNSRC
CLNACC RCV000171358.1,