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rs72551349

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72551349(C;T)
Make rs72551349(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position233767873
GeneUGT1A1, UGT1A3, UGT1A4, UGT1A5, UGT1A6, UGT1A7, UGT1A8, UGT1A9, UGT1A10
is asnp
is mentioned by
dbSNPrs72551349
ebirs72551349
HLIrs72551349
Exacrs72551349
Varsomers72551349
Maprs72551349
PheGenIrs72551349
hapmaprs72551349
1000 genomesrs72551349
hgdprs72551349
ensemblrs72551349
gopubmedrs72551349
geneviewrs72551349
scholarrs72551349
googlers72551349
pharmgkbrs72551349
gwascentralrs72551349
openSNPrs72551349
23andMers72551349
23andMe allrs72551349
SNP Nexus

SNPshotrs72551349
SNPdbers72551349
MSV3drs72551349
GWAS Ctlgrs72551349
Max Magnitude0
OMIM191740
Desc
Variant0004
Relatedalso


ClinVar
Risk rs72551349(T;T)
Alt rs72551349(T;T)
Reference rs72551349(C;C)
Significance Other
Disease Crigler Najjar syndrome Gilbert's syndrome
Variation info
Gene UGT1A5 UGT1A9 UGT1A3 UGT1A6 UGT1A4 UGT1A1 UGT1A10 UGT1A8 UGT1A7
CLNDBN Crigler Najjar syndrome, type 1 Gilbert's syndrome
Reversed 0
HGVS NC_000002.11:g.234676519C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013056.24, RCV000013057.25,