rs587776763

Orientation

plus

Stabilized

plus

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

Make rs587776763(-;T)

Make rs587776763(T;T)

Reference

GRCh38 38.1/142

Chromosome

2

Position

233760761

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

is a	snp
is	mentioned by
dbSNP	rs587776763
dbSNP (classic)	rs587776763
ClinGen	rs587776763
ebi	rs587776763
HLI	rs587776763
Exac	rs587776763
Gnomad	rs587776763
Varsome	rs587776763
LitVar	rs587776763
Map	rs587776763
PheGenI	rs587776763
Biobank	rs587776763
1000 genomes	rs587776763
hgdp	rs587776763
ensembl	rs587776763
geneview	rs587776763
scholar	rs587776763
google	rs587776763
pharmgkb	rs587776763
gwascentral	rs587776763
openSNP	rs587776763
23andMe	rs587776763
SNPshot	rs587776763
SNPdbe	rs587776763
MSV3d	rs587776763
GWAS Ctlg	rs587776763

Max Magnitude

0

ClinVar
Risk	rs587776763(T;T)
Alt	rs587776763(T;T)
Reference	Rs587776763(-;-)
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.234669407_234669408insT
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000013067.16,