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rs146170505

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs146170505(A;A)
Make rs146170505(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position97699370
GeneDPYD
is asnp
is mentioned by
dbSNPrs146170505
dbSNP (classic)rs146170505
ClinGenrs146170505
ebirs146170505
HLIrs146170505
Exacrs146170505
Gnomadrs146170505
Varsomers146170505
LitVarrs146170505
Maprs146170505
PheGenIrs146170505
Biobankrs146170505
1000 genomesrs146170505
hgdprs146170505
ensemblrs146170505
geneviewrs146170505
scholarrs146170505
googlers146170505
pharmgkbrs146170505
gwascentralrs146170505
openSNPrs146170505
23andMers146170505
SNPshotrs146170505
SNPdbers146170505
MSV3drs146170505
GWAS Ctlgrs146170505
Max Magnitude0
ClinVar
Risk rs146170505(A;A)
Alt rs146170505(A;A)
Reference Rs146170505(C;C)
Significance Probable-Pathogenic
Disease Dihydropyrimidine dehydrogenase deficiency
Variation info
Gene DPYD
CLNDBN Dihydropyrimidine dehydrogenase deficiency
Reversed 0
HGVS NC_000001.10:g.98164926C>A
CLNSRC
CLNACC RCV000410667.1,