rs1042640

Orientation

plus

Stabilized

plus

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

Make rs1042640(C;C)

Make rs1042640(C;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

233772898

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

is a	snp
is	mentioned by
dbSNP	rs1042640
dbSNP (classic)	rs1042640
ClinGen	rs1042640
ebi	rs1042640
HLI	rs1042640
Exac	rs1042640
Gnomad	rs1042640
Varsome	rs1042640
LitVar	rs1042640
Map	rs1042640
PheGenI	rs1042640
Biobank	rs1042640
1000 genomes	rs1042640
hgdp	rs1042640
ensembl	rs1042640
geneview	rs1042640
scholar	rs1042640
google	rs1042640
pharmgkb	rs1042640
gwascentral	rs1042640
openSNP	rs1042640
23andMe	rs1042640
SNPshot	rs1042640
SNPdbe	rs1042640
MSV3d	rs1042640
GWAS Ctlg	rs1042640

Max Magnitude

0

?	(C;C) (C;G) (G;G)	28

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

ClinVar
Risk	rs1042640(C;C) rs1042640(T;T)
Alt	rs1042640(C;C) rs1042640(T;T)
Reference	Rs1042640(G;G)
Significance	Non-pathogenic
Disease	Crigler-Najjar syndrome Hyperbilirubinemia transient familial neonatal Gilbert's syndrome
Variation	info
Gene	UGT1A5 UGT1A9 UGT1A3 UGT1A6 UGT1A4 UGT1A1 UGT1A10 UGT1A8 UGT1A7
CLNDBN	Crigler-Najjar syndrome Hyperbilirubinemia transient familial neonatal Gilbert's syndrome
Reversed	0
HGVS	NC_000002.11:g.234681544G>C
CLNSRC
CLNACC	RCV000278221.1, RCV000338732.1, RCV000404223.1,