rs587776764

Orientation

plus

Stabilized

plus

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

Make rs587776764(C;C)

Make rs587776764(C;G)

Reference

GRCh38 38.1/142

Chromosome

2

Position

233761152

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

is a	snp
is	mentioned by
dbSNP	rs587776764
dbSNP (classic)	rs587776764
ClinGen	rs587776764
ebi	rs587776764
HLI	rs587776764
Exac	rs587776764
Gnomad	rs587776764
Varsome	rs587776764
LitVar	rs587776764
Map	rs587776764
PheGenI	rs587776764
Biobank	rs587776764
1000 genomes	rs587776764
hgdp	rs587776764
ensembl	rs587776764
geneview	rs587776764
scholar	rs587776764
google	rs587776764
pharmgkb	rs587776764
gwascentral	rs587776764
openSNP	rs587776764
23andMe	rs587776764
SNPshot	rs587776764
SNPdbe	rs587776764
MSV3d	rs587776764
GWAS Ctlg	rs587776764

Max Magnitude

0

ClinVar
Risk	rs587776764(C;C)
Alt	rs587776764(C;C)
Reference	Rs587776764(G;G)
Significance	Pathogenic
Disease	Crigler Najjar syndrome
Variation	info
Gene	UGT1A5 UGT1A9 UGT1A3 UGT1A6 UGT1A4 UGT1A1 UGT1A10 UGT1A8 UGT1A7
CLNDBN	Crigler Najjar syndrome, type 1
Reversed	0
HGVS	NC_000002.11:g.234669798G>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000013068.24,