rs755218546

Orientation

plus

Stabilized

plus

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

Make rs755218546(A;A)

Make rs755218546(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

233767936

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

is a	snp
is	mentioned by
dbSNP	rs755218546
dbSNP (classic)	rs755218546
ClinGen	rs755218546
ebi	rs755218546
HLI	rs755218546
Exac	rs755218546
Gnomad	rs755218546
Varsome	rs755218546
LitVar	rs755218546
Map	rs755218546
PheGenI	rs755218546
Biobank	rs755218546
1000 genomes	rs755218546
hgdp	rs755218546
ensembl	rs755218546
geneview	rs755218546
scholar	rs755218546
google	rs755218546
pharmgkb	rs755218546
gwascentral	rs755218546
openSNP	rs755218546
23andMe	rs755218546
SNPshot	rs755218546
SNPdbe	rs755218546
MSV3d	rs755218546
GWAS Ctlg	rs755218546

Max Magnitude

0

ClinVar
Risk	rs755218546(A;A)
Alt	rs755218546(A;A)
Reference	Rs755218546(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	UGT1A5 UGT1A3 UGT1A9 UGT1A6 UGT1A4 UGT1A1 UGT1A8 UGT1A10 UGT1A7
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.234676582G>A
CLNSRC
CLNACC	RCV000482866.1,