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rs587776761

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TACATTAATGCTTC;TACATTAATGCTTC) 0 common in clinvar
Make rs587776761(A;A)
Make rs587776761(A;TACATTAATGCTTC)
ReferenceGRCh38 38.1/142
Chromosome2
Position233767046
GeneUGT1A1, UGT1A3, UGT1A4, UGT1A5, UGT1A6, UGT1A7, UGT1A8, UGT1A9, UGT1A10
is asnp
is mentioned by
dbSNPrs587776761
dbSNP (old)rs587776761
ClinGenrs587776761
ebirs587776761
HLIrs587776761
Exacrs587776761
Gnomadrs587776761
Varsomers587776761
Maprs587776761
PheGenIrs587776761
Biobankrs587776761
1000 genomesrs587776761
hgdprs587776761
ensemblrs587776761
gopubmedrs587776761
geneviewrs587776761
scholarrs587776761
googlers587776761
pharmgkbrs587776761
gwascentralrs587776761
openSNPrs587776761
23andMers587776761
23andMe allrs587776761
SNP Nexus

SNPshotrs587776761
SNPdbers587776761
MSV3drs587776761
GWAS Ctlgrs587776761
Max Magnitude0
ClinVar
Risk rs587776761(A;A)
Alt rs587776761(A;A)
Reference Rs587776761(TACATTAATGCTTC;TACATTAATGCTTC)
Significance Pathogenic
Disease Crigler Najjar syndrome
Variation info
Gene UGT1A5 UGT1A3 UGT1A9 UGT1A6 UGT1A4 UGT1A1 UGT1A10 UGT1A8 UGT1A7
CLNDBN Crigler Najjar syndrome, type 1
Reversed 0
HGVS NC_000002.11:g.234675692_234675705delTACATTAATGCTTCinsA
CLNSRC OMIM Allelic Variant
CLNACC RCV000013053.23,