rs587776765

Orientation

plus

Stabilized

plus

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

Make rs587776765(C;T)

Make rs587776765(T;T)

Reference

GRCh38 38.1/142

Chromosome

2

Position

233760432

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

is a	snp
is	mentioned by
dbSNP	rs587776765
dbSNP (classic)	rs587776765
ClinGen	rs587776765
ebi	rs587776765
HLI	rs587776765
Exac	rs587776765
Gnomad	rs587776765
Varsome	rs587776765
LitVar	rs587776765
Map	rs587776765
PheGenI	rs587776765
Biobank	rs587776765
1000 genomes	rs587776765
hgdp	rs587776765
ensembl	rs587776765
geneview	rs587776765
scholar	rs587776765
google	rs587776765
pharmgkb	rs587776765
gwascentral	rs587776765
openSNP	rs587776765
23andMe	rs587776765
SNPshot	rs587776765
SNPdbe	rs587776765
MSV3d	rs587776765
GWAS Ctlg	rs587776765

Max Magnitude

0

ClinVar
Risk	rs587776765(T;T)
Alt	rs587776765(T;T)
Reference	Rs587776765(C;C)
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.234669078C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000013069.25,