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rs114982090

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs114982090(C;T)
Make rs114982090(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position233772309
GeneUGT1A1, UGT1A3, UGT1A4, UGT1A5, UGT1A6, UGT1A7, UGT1A8, UGT1A9, UGT1A10
is asnp
is mentioned by
dbSNPrs114982090
ebirs114982090
HLIrs114982090
Exacrs114982090
Varsomers114982090
Maprs114982090
PheGenIrs114982090
hapmaprs114982090
1000 genomesrs114982090
hgdprs114982090
ensemblrs114982090
gopubmedrs114982090
geneviewrs114982090
scholarrs114982090
googlers114982090
pharmgkbrs114982090
gwascentralrs114982090
openSNPrs114982090
23andMers114982090
23andMe allrs114982090
SNP Nexus

SNPshotrs114982090
SNPdbers114982090
MSV3drs114982090
GWAS Ctlgrs114982090
Max Magnitude0

[PMID 24856997] [Mutations in UGT1A1 gene in neonates with hyperbilirubinemia of Guangxi Heiyi Zhuang nationality]

ClinVar
Risk rs114982090(T;T)
Alt rs114982090(T;T)
Reference rs114982090(C;C)
Significance Unknown
Disease not provided
Variation info
Gene UGT1A5 UGT1A9 UGT1A3 UGT1A6 UGT1A4 UGT1A1 UGT1A8 UGT1A10 UGT1A7
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.234680955C>T
CLNSRC
CLNACC RCV000178772.1,