rs35350960

Orientation

plus

Stabilized

plus

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

Make rs35350960(A;A)

Make rs35350960(A;C)

Reference

GRCh38 38.1/141

Chromosome

2

Position

233760973

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

is a	snp
is	mentioned by
dbSNP	rs35350960
dbSNP (classic)	rs35350960
ClinGen	rs35350960
ebi	rs35350960
HLI	rs35350960
Exac	rs35350960
Gnomad	rs35350960
Varsome	rs35350960
LitVar	rs35350960
Map	rs35350960
PheGenI	rs35350960
Biobank	rs35350960
1000 genomes	rs35350960
hgdp	rs35350960
ensembl	rs35350960
geneview	rs35350960
scholar	rs35350960
google	rs35350960
pharmgkb	rs35350960
gwascentral	rs35350960
openSNP	rs35350960
23andMe	rs35350960
SNPshot	rs35350960
SNPdbe	rs35350960
MSV3d	rs35350960
GWAS Ctlg	rs35350960

GMAF

0.0004591

Max Magnitude

0

OMIM	191740
Desc
Variant	0010
Related	also

ClinVar
Risk	rs35350960(A;A) rs35350960(T;T)
Alt	rs35350960(A;A) rs35350960(T;T)
Reference	Rs35350960(C;C)
Significance	Other
Disease	Gilbert's syndrome Crigler-Najjar syndrome not specified not provided
Variation	info
Gene	UGT1A5 UGT1A9 UGT1A3 UGT1A6 UGT1A4 UGT1A1 UGT1A10 UGT1A8 UGT1A7
CLNDBN	Gilbert's syndrome Crigler-Najjar syndrome, type II not specified not provided
Reversed	0
HGVS	NC_000002.11:g.234669619C>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000013062.23, RCV000013063.24, RCV000147905.1, RCV000299521.1,

[PMID 18547414] Genotyping panel for assessing response to cancer chemotherapy.