rs62625011

Orientation

plus

Stabilized

plus

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

Make rs62625011(A;A)

Make rs62625011(A;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

233767092

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

is a	snp
is	mentioned by
dbSNP	rs62625011
dbSNP (classic)	rs62625011
ClinGen	rs62625011
ebi	rs62625011
HLI	rs62625011
Exac	rs62625011
Gnomad	rs62625011
Varsome	rs62625011
LitVar	rs62625011
Map	rs62625011
PheGenI	rs62625011
Biobank	rs62625011
1000 genomes	rs62625011
hgdp	rs62625011
ensembl	rs62625011
geneview	rs62625011
scholar	rs62625011
google	rs62625011
pharmgkb	rs62625011
gwascentral	rs62625011
openSNP	rs62625011
23andMe	rs62625011
SNPshot	rs62625011
SNPdbe	rs62625011
MSV3d	rs62625011
GWAS Ctlg	rs62625011

Max Magnitude

0

ClinVar
Risk	rs62625011(A;A)
Alt	rs62625011(A;A)
Reference	Rs62625011(G;G)
Significance	Pathogenic
Disease	Crigler Najjar syndrome
Variation	info
Gene	UGT1A5 UGT1A3 UGT1A9 UGT1A6 UGT1A4 UGT1A1 UGT1A8 UGT1A10 UGT1A7
CLNDBN	Crigler Najjar syndrome, type 1
Reversed	0
HGVS	NC_000002.11:g.234675738G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000013060.24,