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rs587776762

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TTC;TTC) 0 common in clinvar
Make rs587776762(-;-)
Make rs587776762(-;CTT)
Make rs587776762(CTT;CTT)
ReferenceGRCh38 38.1/142
Chromosome2
Position233760800
GeneUGT1A1, UGT1A3, UGT1A4, UGT1A5, UGT1A6, UGT1A7, UGT1A8, UGT1A9, UGT1A10
is asnp
is mentioned by
dbSNPrs587776762
ebirs587776762
HLIrs587776762
Exacrs587776762
Varsomers587776762
Maprs587776762
PheGenIrs587776762
hapmaprs587776762
1000 genomesrs587776762
hgdprs587776762
ensemblrs587776762
gopubmedrs587776762
geneviewrs587776762
scholarrs587776762
googlers587776762
pharmgkbrs587776762
gwascentralrs587776762
openSNPrs587776762
23andMers587776762
23andMe allrs587776762
SNP Nexus

SNPshotrs587776762
SNPdbers587776762
MSV3drs587776762
GWAS Ctlgrs587776762
Max Magnitude0
ClinVar
Risk rs587776762(;)
Alt rs587776762(;)
Reference rs587776762(TTC;TTC)
Significance Pathogenic
Disease Crigler Najjar syndrome
Variation info
Gene UGT1A5 UGT1A3 UGT1A9 UGT1A6 UGT1A4 UGT1A1 UGT1A8 UGT1A10 UGT1A7
CLNDBN Crigler Najjar syndrome, type 1
Reversed 0
HGVS NC_000002.11:g.234669446_234669448delCTT
CLNSRC OMIM Allelic Variant
CLNACC RCV000013059.24,