rs114982090

Orientation

plus

Stabilized

plus

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

Make rs114982090(C;T)

Make rs114982090(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

233772309

Gene	MROH2A, UGT1A1, UGT1A10, UGT1A3, UGT1A4, UGT1A5, UGT1A6, UGT1A7, UGT1A8, UGT1A9

is a	snp
is	mentioned by
dbSNP	rs114982090
dbSNP (classic)	rs114982090
ClinGen	rs114982090
ebi	rs114982090
HLI	rs114982090
Exac	rs114982090
Gnomad	rs114982090
Varsome	rs114982090
LitVar	rs114982090
Map	rs114982090
PheGenI	rs114982090
Biobank	rs114982090
1000 genomes	rs114982090
hgdp	rs114982090
ensembl	rs114982090
geneview	rs114982090
scholar	rs114982090
google	rs114982090
pharmgkb	rs114982090
gwascentral	rs114982090
openSNP	rs114982090
23andMe	rs114982090
SNPshot	rs114982090
SNPdbe	rs114982090
MSV3d	rs114982090
GWAS Ctlg	rs114982090

Max Magnitude

0

[PMID 24856997] [Mutations in UGT1A1 gene in neonates with hyperbilirubinemia of Guangxi Heiyi Zhuang nationality]

ClinVar
Risk	rs114982090(T;T)
Alt	rs114982090(T;T)
Reference	Rs114982090(C;C)
Significance	Unknown
Disease	not specified
Variation	info
Gene	UGT1A5 UGT1A3 UGT1A9 UGT1A6 UGT1A4 UGT1A1 UGT1A8 UGT1A10 UGT1A7
CLNDBN	not specified
Reversed	0
HGVS	NC_000002.11:g.234680955C>T
CLNSRC
CLNACC	RCV000178772.1,