rs28934877

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs28934877(A;G)

Make rs28934877(G;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

233768333

Gene	UGT1A1, UGT1A3, UGT1A4, UGT1A5, UGT1A6, UGT1A7, UGT1A8, UGT1A9, UGT1A10

is a	snp
is	mentioned by
dbSNP	rs28934877
dbSNP (classic)	rs28934877
ClinGen	rs28934877
ebi	rs28934877
HLI	rs28934877
Exac	rs28934877
Gnomad	rs28934877
Varsome	rs28934877
LitVar	rs28934877
Map	rs28934877
PheGenI	rs28934877
Biobank	rs28934877
1000 genomes	rs28934877
hgdp	rs28934877
ensembl	rs28934877
geneview	rs28934877
scholar	rs28934877
google	rs28934877
pharmgkb	rs28934877
gwascentral	rs28934877
openSNP	rs28934877
23andMe	rs28934877
SNPshot	rs28934877
SNPdbe	rs28934877
MSV3d	rs28934877
GWAS Ctlg	rs28934877

Merged from

Rs111033540, Rs386576623

Max Magnitude

0

OMIM	191740
Desc	CRIGLER-NAJJAR SYNDROME, TYPE II
Variant	0022
Related	also

[PMID 19572200] Prediction of deleterious non-synonymous single-nucleotide polymorphisms of human uridine diphosphate glucuronosyltransferase genes.

ClinVar
Risk	rs28934877(C;C) rs28934877(G;G)
Alt	rs28934877(C;C) rs28934877(G;G)
Reference	Rs28934877(A;A)
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 II Gilbert's syndrome
Reversed	0
HGVS	NC_000002.11:g.234676979A>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000013079.17, RCV000013080.25,