rs797045637

Orientation

minus

Stabilized

minus

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

Make rs797045637(C;C)

Make rs797045637(C;G)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

17387226

Gene

KCNJ11

is a	snp
is	mentioned by
dbSNP	rs797045637
dbSNP (classic)	rs797045637
ClinGen	rs797045637
ebi	rs797045637
HLI	rs797045637
Exac	rs797045637
Gnomad	rs797045637
Varsome	rs797045637
LitVar	rs797045637
Map	rs797045637
PheGenI	rs797045637
Biobank	rs797045637
1000 genomes	rs797045637
hgdp	rs797045637
ensembl	rs797045637
geneview	rs797045637
scholar	rs797045637
google	rs797045637
pharmgkb	rs797045637
gwascentral	rs797045637
openSNP	rs797045637
23andMe	rs797045637
SNPshot	rs797045637
SNPdbe	rs797045637
MSV3d	rs797045637
GWAS Ctlg	rs797045637

Max Magnitude

0

ClinVar
Risk	rs797045637(C;C) rs797045637(T;T)
Alt	rs797045637(C;C) rs797045637(T;T)
Reference	Rs797045637(G;G)
Significance	Probable-Pathogenic
Disease	Islet cell hyperplasia
Variation	info
Gene	KCNJ11
CLNDBN	Islet cell hyperplasia
Reversed	1
HGVS	NC_000011.9:g.17408773C>A; NC_000011.9:g.17408773C>G
CLNSRC
CLNACC	RCV000194466.1, RCV000193250.1,