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rs886039771

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs886039771(-;A)
Make rs886039771(A;A)
ReferenceGRCh38.p7 38.3/149
Chromosome2
Position233760640
GeneUGT1A1, UGT1A3, UGT1A4, UGT1A5, UGT1A6, UGT1A7, UGT1A8, UGT1A9, UGT1A10
is asnp
is mentioned by
dbSNPrs886039771
dbSNP (classic)rs886039771
ClinGenrs886039771
ebirs886039771
HLIrs886039771
Exacrs886039771
Gnomadrs886039771
Varsomers886039771
LitVarrs886039771
Maprs886039771
PheGenIrs886039771
Biobankrs886039771
1000 genomesrs886039771
hgdprs886039771
ensemblrs886039771
geneviewrs886039771
scholarrs886039771
googlers886039771
pharmgkbrs886039771
gwascentralrs886039771
openSNPrs886039771
23andMers886039771
23andMe allrs886039771
SNPshotrs886039771
SNPdbers886039771
MSV3drs886039771
GWAS Ctlgrs886039771
Max Magnitude0
ClinVar
Risk rs886039771(A;A)
Alt rs886039771(A;A)
Reference Rs886039771(-;-)
Significance Probable-Pathogenic
Disease Crigler-Najjar syndrome
Variation info
Gene UGT1A5 UGT1A9 UGT1A3 UGT1A6 UGT1A4 UGT1A1 UGT1A8 UGT1A10 UGT1A7
CLNDBN Crigler-Najjar syndrome
Reversed 0
HGVS NC_000002.11:g.234669286dupA
CLNSRC
CLNACC RCV000256423.1,