rs797046091

Orientation

plus

Stabilized

plus

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

Make rs797046091(-;-)

Make rs797046091(-;AG)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

233761009

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

is a	snp
is	mentioned by
dbSNP	rs797046091
dbSNP (classic)	rs797046091
ClinGen	rs797046091
ebi	rs797046091
HLI	rs797046091
Exac	rs797046091
Gnomad	rs797046091
Varsome	rs797046091
LitVar	rs797046091
Map	rs797046091
PheGenI	rs797046091
Biobank	rs797046091
1000 genomes	rs797046091
hgdp	rs797046091
ensembl	rs797046091
geneview	rs797046091
scholar	rs797046091
google	rs797046091
pharmgkb	rs797046091
gwascentral	rs797046091
openSNP	rs797046091
23andMe	rs797046091
SNPshot	rs797046091
SNPdbe	rs797046091
MSV3d	rs797046091
GWAS Ctlg	rs797046091

Max Magnitude

0

ClinVar
Risk	rs797046091(-;-)
Alt	rs797046091(-;-)
Reference	Rs797046091(AG;AG)
Significance	Pathogenic
Disease	Hyperbilirubinemia
Variation	info
Gene	UGT1A5 UGT1A3 UGT1A9 UGT1A6 UGT1A4 UGT1A1 UGT1A8 UGT1A10 UGT1A7
CLNDBN	Hyperbilirubinemia
Reversed	0
HGVS	NC_000002.11:g.234669655_234669656delAG
CLNSRC
CLNACC	RCV000194838.1,