rs780957825

Orientation

plus

Stabilized

plus

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

Make rs780957825(A;A)

Make rs780957825(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

17387211

Gene

KCNJ11

is a	snp
is	mentioned by
dbSNP	rs780957825
dbSNP (classic)	rs780957825
ClinGen	rs780957825
ebi	rs780957825
HLI	rs780957825
Exac	rs780957825
Gnomad	rs780957825
Varsome	rs780957825
LitVar	rs780957825
Map	rs780957825
PheGenI	rs780957825
Biobank	rs780957825
1000 genomes	rs780957825
hgdp	rs780957825
ensembl	rs780957825
geneview	rs780957825
scholar	rs780957825
google	rs780957825
pharmgkb	rs780957825
gwascentral	rs780957825
openSNP	rs780957825
23andMe	rs780957825
SNPshot	rs780957825
SNPdbe	rs780957825
MSV3d	rs780957825
GWAS Ctlg	rs780957825

Max Magnitude

0

ClinVar
Risk	rs780957825(A;A)
Alt	rs780957825(A;A)
Reference	Rs780957825(G;G)
Significance	Pathogenic
Disease	Islet cell hyperplasia
Variation	info
Gene	KCNJ11
CLNDBN	Islet cell hyperplasia
Reversed	0
HGVS	NC_000011.9:g.17408758G>A
CLNSRC
CLNACC	RCV000192330.1,