rs587776762

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(CTT;CTT)	0	common in clinvar
(I;I)	0	common genotype
(TTC;TTC)	0	common in clinvar

Make rs587776762(-;-)

Make rs587776762(-;CTT)

Reference

GRCh38 38.1/142

Chromosome

2

Position

233760800

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

is a	snp
is	mentioned by
dbSNP	rs587776762
dbSNP (classic)	rs587776762
ClinGen	rs587776762
ebi	rs587776762
HLI	rs587776762
Exac	rs587776762
Gnomad	rs587776762
Varsome	rs587776762
LitVar	rs587776762
Map	rs587776762
PheGenI	rs587776762
Biobank	rs587776762
1000 genomes	rs587776762
hgdp	rs587776762
ensembl	rs587776762
geneview	rs587776762
scholar	rs587776762
google	rs587776762
pharmgkb	rs587776762
gwascentral	rs587776762
openSNP	rs587776762
23andMe	rs587776762
SNPshot	rs587776762
SNPdbe	rs587776762
MSV3d	rs587776762
GWAS Ctlg	rs587776762

Merged from

Rs281875379

Max Magnitude

0

ClinVar
Risk	rs587776762(-;-) Rs587776762(TTC;TTC)
Alt	rs587776762(-;-) Rs587776762(TTC;TTC)
Reference	Rs587776762(CTT;CTT)
Significance	Pathogenic
Disease	Crigler Najjar syndrome
Variation	info
Gene	UGT1A5 UGT1A9 UGT1A3 UGT1A6 UGT1A4 UGT1A1 UGT1A10 UGT1A8 UGT1A7
CLNDBN	Crigler Najjar syndrome, type 1
Reversed	0
HGVS	NC_000002.11:g.234669446_234669448delCTT
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000013059.24,