rs886039771

Orientation

plus

Stabilized

plus

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

Make rs886039771(-;A)

Make rs886039771(A;A)

Reference

GRCh38.p7 38.3/149

Chromosome

2

Position

233760640

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

is a	snp
is	mentioned by
dbSNP	rs886039771
dbSNP (classic)	rs886039771
ClinGen	rs886039771
ebi	rs886039771
HLI	rs886039771
Exac	rs886039771
Gnomad	rs886039771
Varsome	rs886039771
LitVar	rs886039771
Map	rs886039771
PheGenI	rs886039771
Biobank	rs886039771
1000 genomes	rs886039771
hgdp	rs886039771
ensembl	rs886039771
geneview	rs886039771
scholar	rs886039771
google	rs886039771
pharmgkb	rs886039771
gwascentral	rs886039771
openSNP	rs886039771
23andMe	rs886039771
SNPshot	rs886039771
SNPdbe	rs886039771
MSV3d	rs886039771
GWAS Ctlg	rs886039771

Max Magnitude

0

ClinVar
Risk	rs886039771(A;A)
Alt	rs886039771(A;A)
Reference	Rs886039771(-;-)
Significance	Probable-Pathogenic
Disease	Crigler-Najjar syndrome
Variation	info
Gene	UGT1A5 UGT1A9 UGT1A3 UGT1A6 UGT1A4 UGT1A1 UGT1A8 UGT1A10 UGT1A7
CLNDBN	Crigler-Najjar syndrome
Reversed	0
HGVS	NC_000002.11:g.234669286dupA
CLNSRC
CLNACC	RCV000256423.1,