rs797046090

Orientation

plus

Stabilized

plus

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

Make rs797046090(-;GTAC)

Make rs797046090(GTAC;GTAC)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

233760525

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

is a	snp
is	mentioned by
dbSNP	rs797046090
dbSNP (classic)	rs797046090
ClinGen	rs797046090
ebi	rs797046090
HLI	rs797046090
Exac	rs797046090
Gnomad	rs797046090
Varsome	rs797046090
LitVar	rs797046090
Map	rs797046090
PheGenI	rs797046090
Biobank	rs797046090
1000 genomes	rs797046090
hgdp	rs797046090
ensembl	rs797046090
geneview	rs797046090
scholar	rs797046090
google	rs797046090
pharmgkb	rs797046090
gwascentral	rs797046090
openSNP	rs797046090
23andMe	rs797046090
SNPshot	rs797046090
SNPdbe	rs797046090
MSV3d	rs797046090
GWAS Ctlg	rs797046090

Max Magnitude

0

ClinVar
Risk	rs797046090(CGTA;CGTA)
Alt	rs797046090(CGTA;CGTA)
Reference	Rs797046090(-;-)
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.234669171_234669172insGTAC
CLNSRC
CLNACC	RCV000193803.1,