rs11045819

plus

Geno	Mag	Summary
(C;C)	0	common on affy axiom data

Make rs11045819(A;A)

Make rs11045819(A;C)

Reference

GRCh38 38.1/141

Chromosome

12

Position

21176879

Gene

SLCO1B1

is a	snp
is	mentioned by
dbSNP	rs11045819
dbSNP (classic)	rs11045819
ClinGen	rs11045819
ebi	rs11045819
HLI	rs11045819
Exac	rs11045819
Gnomad	rs11045819
Varsome	rs11045819
LitVar	rs11045819
Map	rs11045819
PheGenI	rs11045819
Biobank	rs11045819
1000 genomes	rs11045819
hgdp	rs11045819
ensembl	rs11045819
geneview	rs11045819
scholar	rs11045819
google	rs11045819
pharmgkb	rs11045819
gwascentral	rs11045819
openSNP	rs11045819
23andMe	rs11045819
SNPshot	rs11045819
SNPdbe	rs11045819
MSV3d	rs11045819
GWAS Ctlg	rs11045819

GMAF

0.07851

Max Magnitude

0

?

(A;A) (A;C) (C;C)

28

[PMID 20139798] ADME pharmacogenetics: investigation of the pharmacokinetics of the antiretroviral agent lopinavir coformulated with ritonavir.

[PMID 20973885] Organic anion transporter 1B1 (SLCO1B1) polymorphism and gallstone formation: High incidence of Exon4 CA genotype in female patients in North India.

[PMID 22136368] Influence of genomic ancestry on the distribution of SLCO1B1, SLCO1B3 and ABCB1 gene polymorphisms among Brazilians.

[PMID 23100282 ] Impact of common genetic variation on response to simvastatin therapy among 18 705 participants in the Heart Protection Study.

[PMID 23133420 ] Pharmacogenomic Diversity among Brazilians: Influence of Ancestry, Self-Reported Color, and Geographical Origin.

ClinVar
Risk	rs11045819(A;A)
Alt	rs11045819(A;A)
Reference	Rs11045819(C;C)
Significance	Probable-non-pathogenic
Disease	Rotor syndrome
Variation	info
Gene	SLCO1B1
CLNDBN	Rotor syndrome
Reversed	0
HGVS	NC_000012.11:g.21329813C>A
CLNSRC
CLNACC	RCV000364840.1,