Rs28934877

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Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs28934877(A;G)
Make rs28934877(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position233768333
GeneUGT1A1, UGT1A3, UGT1A4, UGT1A5, UGT1A6, UGT1A7, UGT1A8, UGT1A9, UGT1A10
is asnp
is mentioned by
dbSNPrs28934877
Exacrs28934877
PheGenIrs28934877
nextbiors28934877
hapmaprs28934877
1000 genomesrs28934877
hgdprs28934877
ensemblrs28934877
gopubmedrs28934877
geneviewrs28934877
scholarrs28934877
googlers28934877
pharmgkbrs28934877
gwascentralrs28934877
openSNPrs28934877
23andMers28934877
23andMe allrs28934877
SNP Nexus

SNPshotrs28934877
SNPdbers28934877
MSV3drs28934877
Merged fromRs111033540
Max Magnitude0
OMIM191740
DescCRIGLER-NAJJAR SYNDROME, TYPE II
Variant0022
Relatedalso
[PMID 19572200OA-icon.png] Prediction of deleterious non-synonymous single-nucleotide polymorphisms of human uridine diphosphate glucuronosyltransferase genes.


ClinVar
Risk rs28934877(C,G;C,G)
Alt rs28934877(C,G;C,G)
Reference rs28934877(A;A)
Significance Pathogenic
Disease Crigler-Najjar syndrome Gilbert's syndrome
Variation info
Gene UGT1A5 UGT1A9 UGT1A3 UGT1A6 UGT1A4 UGT1A1 UGT1A8 UGT1A10 UGT1A7
CLNDBN Crigler-Najjar syndrome, type II Gilbert's syndrome
Reversed 0
HGVS NC_000002.11:g.234676979A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000013079.15, RCV000013080.22,