rs34946978

Orientation

plus

Stabilized

plus

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

Make rs34946978(C;T)

Make rs34946978(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

233768226

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

is a	snp
is	mentioned by
dbSNP	rs34946978
dbSNP (classic)	rs34946978
ClinGen	rs34946978
ebi	rs34946978
HLI	rs34946978
Exac	rs34946978
Gnomad	rs34946978
Varsome	rs34946978
LitVar	rs34946978
Map	rs34946978
PheGenI	rs34946978
Biobank	rs34946978
1000 genomes	rs34946978
hgdp	rs34946978
ensembl	rs34946978
geneview	rs34946978
scholar	rs34946978
google	rs34946978
pharmgkb	rs34946978
gwascentral	rs34946978
openSNP	rs34946978
23andMe	rs34946978
SNPshot	rs34946978
SNPdbe	rs34946978
MSV3d	rs34946978
GWAS Ctlg	rs34946978

Max Magnitude

0

ClinVar
Risk	rs34946978(T;T)
Alt	rs34946978(T;T)
Reference	Rs34946978(C;C)
Significance	Other
Disease	Hyperbilirubinemia not provided
Variation	info
Gene	UGT1A5 UGT1A3 UGT1A9 UGT1A6 UGT1A4 UGT1A1 UGT1A8 UGT1A10 UGT1A7
CLNDBN	Hyperbilirubinemia not provided
Reversed	0
HGVS	NC_000002.11:g.234676872C>T
CLNSRC
CLNACC	RCV000194762.1, RCV000300556.2,