rs1800467

Orientation

minus

Stabilized

minus

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

Make rs1800467(C;G)

Make rs1800467(G;G)

Reference

GRCh38 38.1/142

Chromosome

11

Position

17387284

Gene

KCNJ11

is a	snp
is	mentioned by
dbSNP	rs1800467
dbSNP (classic)	rs1800467
ClinGen	rs1800467
ebi	rs1800467
HLI	rs1800467
Exac	rs1800467
Gnomad	rs1800467
Varsome	rs1800467
LitVar	rs1800467
Map	rs1800467
PheGenI	rs1800467
Biobank	rs1800467
1000 genomes	rs1800467
hgdp	rs1800467
ensembl	rs1800467
geneview	rs1800467
scholar	rs1800467
google	rs1800467
pharmgkb	rs1800467
gwascentral	rs1800467
openSNP	rs1800467
23andMe	rs1800467
SNPshot	rs1800467
SNPdbe	rs1800467
MSV3d	rs1800467
GWAS Ctlg	rs1800467

Max Magnitude

0

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

[PMID 25247988] Population Specific Impact of Genetic Variants in KCNJ11 Gene to Type 2 Diabetes: A Case-Control and Meta-Analysis Study

ClinVar
Risk	rs1800467(A;A) rs1800467(G;G)
Alt	rs1800467(A;A) rs1800467(G;G)
Reference	Rs1800467(C;C)
Significance	Probable-non-pathogenic
Disease	not specified Hyperinsulinism Transient Neonatal Diabetes Maturity-onset diabetes of the young Monogenic diabetes
Variation	info
Gene	KCNJ11
CLNDBN	not specified Hyperinsulinism, Dominant/Recessive Transient Neonatal Diabetes, Dominant Maturity-onset diabetes of the young Monogenic diabetes
Reversed	1
HGVS	NC_000011.9:g.17408831G>C
CLNSRC	ClinVar University of Chicago
CLNACC	RCV000146119.3, RCV000285092.1, RCV000323784.1, RCV000372639.1, RCV000445429.1,

[PMID 25733456] Genetic Variations in Magnesium-Related Ion Channels May Affect Diabetes Risk among African American and Hispanic American Women