rs587784535

Orientation

plus

Stabilized

plus

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

Make rs587784535(G;T)

Make rs587784535(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

233767937

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

is a	snp
is	mentioned by
dbSNP	rs587784535
dbSNP (classic)	rs587784535
ClinGen	rs587784535
ebi	rs587784535
HLI	rs587784535
Exac	rs587784535
Gnomad	rs587784535
Varsome	rs587784535
LitVar	rs587784535
Map	rs587784535
PheGenI	rs587784535
Biobank	rs587784535
1000 genomes	rs587784535
hgdp	rs587784535
ensembl	rs587784535
geneview	rs587784535
scholar	rs587784535
google	rs587784535
pharmgkb	rs587784535
gwascentral	rs587784535
openSNP	rs587784535
23andMe	rs587784535
SNPshot	rs587784535
SNPdbe	rs587784535
MSV3d	rs587784535
GWAS Ctlg	rs587784535

Max Magnitude

0

ClinVar
Risk	rs587784535(T;T)
Alt	rs587784535(T;T)
Reference	Rs587784535(G;G)
Significance	Pathogenic
Disease	Hyperbilirubinemia
Variation	info
Gene	UGT1A5 UGT1A9 UGT1A3 UGT1A6 UGT1A4 UGT1A1 UGT1A8 UGT1A10 UGT1A7
CLNDBN	Hyperbilirubinemia
Reversed	0
HGVS	NC_000002.11:g.234676583G>T
CLNSRC
CLNACC	RCV000147893.1,