rs587776766

Orientation

plus

Stabilized

plus

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

Make rs587776766(A;G)

Make rs587776766(G;G)

Reference

GRCh38 38.1/142

Chromosome

2

Position

233768218

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

is a	snp
is	mentioned by
dbSNP	rs587776766
dbSNP (classic)	rs587776766
ClinGen	rs587776766
ebi	rs587776766
HLI	rs587776766
Exac	rs587776766
Gnomad	rs587776766
Varsome	rs587776766
LitVar	rs587776766
Map	rs587776766
PheGenI	rs587776766
Biobank	rs587776766
1000 genomes	rs587776766
hgdp	rs587776766
ensembl	rs587776766
geneview	rs587776766
scholar	rs587776766
google	rs587776766
pharmgkb	rs587776766
gwascentral	rs587776766
openSNP	rs587776766
23andMe	rs587776766
SNPshot	rs587776766
SNPdbe	rs587776766
MSV3d	rs587776766
GWAS Ctlg	rs587776766

Max Magnitude

0

ClinVar
Risk	rs587776766(G;G)
Alt	rs587776766(G;G)
Reference	Rs587776766(A;A)
Significance	Pathogenic
Disease	Crigler Najjar syndrome
Variation	info
Gene	UGT1A5 UGT1A3 UGT1A9 UGT1A6 UGT1A4 UGT1A1 UGT1A10 UGT1A8 UGT1A7
CLNDBN	Crigler Najjar syndrome, type 1
Reversed	0
HGVS	NC_000002.11:g.234676864A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000013070.23,