rs72551349

Orientation

plus

Stabilized

plus

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

Make rs72551349(C;T)

Make rs72551349(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

233767873

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

is a	snp
is	mentioned by
dbSNP	rs72551349
dbSNP (classic)	rs72551349
ClinGen	rs72551349
ebi	rs72551349
HLI	rs72551349
Exac	rs72551349
Gnomad	rs72551349
Varsome	rs72551349
LitVar	rs72551349
Map	rs72551349
PheGenI	rs72551349
Biobank	rs72551349
1000 genomes	rs72551349
hgdp	rs72551349
ensembl	rs72551349
geneview	rs72551349
scholar	rs72551349
google	rs72551349
pharmgkb	rs72551349
gwascentral	rs72551349
openSNP	rs72551349
23andMe	rs72551349
SNPshot	rs72551349
SNPdbe	rs72551349
MSV3d	rs72551349
GWAS Ctlg	rs72551349

Max Magnitude

0

OMIM	191740
Desc
Variant	0004
Related	also

ClinVar
Risk	rs72551349(T;T)
Alt	rs72551349(T;T)
Reference	Rs72551349(C;C)
Significance	Other
Disease	Crigler Najjar syndrome Gilbert's syndrome
Variation	info
Gene	UGT1A5 UGT1A3 UGT1A9 UGT1A6 UGT1A4 UGT1A1 UGT1A10 UGT1A8 UGT1A7
CLNDBN	Crigler Najjar syndrome, type 1 Gilbert's syndrome
Reversed	0
HGVS	NC_000002.11:g.234676519C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000013056.24, RCV000013057.25,