rs35003977

Orientation

plus

Stabilized

plus

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

Make rs35003977(G;G)

Make rs35003977(G;T)

Reference

GRCh38.p7 38.3/149

Chromosome

2

Position

233760961

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

is a	snp
is	mentioned by
dbSNP	rs35003977
dbSNP (classic)	rs35003977
ClinGen	rs35003977
ebi	rs35003977
HLI	rs35003977
Exac	rs35003977
Gnomad	rs35003977
Varsome	rs35003977
LitVar	rs35003977
Map	rs35003977
PheGenI	rs35003977
Biobank	rs35003977
1000 genomes	rs35003977
hgdp	rs35003977
ensembl	rs35003977
geneview	rs35003977
scholar	rs35003977
google	rs35003977
pharmgkb	rs35003977
gwascentral	rs35003977
openSNP	rs35003977
23andMe	rs35003977
SNPshot	rs35003977
SNPdbe	rs35003977
MSV3d	rs35003977
GWAS Ctlg	rs35003977

Max Magnitude

0

ClinVar
Risk	rs35003977(G;G)
Alt	rs35003977(G;G)
Reference	Rs35003977(T;T)
Significance	Probable-Pathogenic
Disease	Hyperbilirubinemia Gilbert's syndrome Crigler-Najjar syndrome Hyperbilirubinemia transient familial neonatal
Variation	info
Gene	UGT1A5 UGT1A9 UGT1A3 UGT1A6 UGT1A4 UGT1A1 UGT1A8 UGT1A10 UGT1A7
CLNDBN	Hyperbilirubinemia Gilbert's syndrome Crigler-Najjar syndrome Hyperbilirubinemia transient familial neonatal
Reversed	0
HGVS	NC_000002.11:g.234669607T>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000147904.1, RCV000313763.1, RCV000348706.1, RCV000396791.1,