rs387906398

Orientation

minus

Stabilized

minus

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

Make rs387906398(G;T)

Make rs387906398(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

17388225

Gene

KCNJ11

is a	snp
is	mentioned by
dbSNP	rs387906398
dbSNP (classic)	rs387906398
ClinGen	rs387906398
ebi	rs387906398
HLI	rs387906398
Exac	rs387906398
Gnomad	rs387906398
Varsome	rs387906398
LitVar	rs387906398
Map	rs387906398
PheGenI	rs387906398
Biobank	rs387906398
1000 genomes	rs387906398
hgdp	rs387906398
ensembl	rs387906398
geneview	rs387906398
scholar	rs387906398
google	rs387906398
pharmgkb	rs387906398
gwascentral	rs387906398
openSNP	rs387906398
23andMe	rs387906398
SNPshot	rs387906398
SNPdbe	rs387906398
MSV3d	rs387906398
GWAS Ctlg	rs387906398

Max Magnitude

0

ClinVar
Risk	rs387906398(T;T)
Alt	rs387906398(T;T)
Reference	Rs387906398(G;G)
Significance	Pathogenic
Disease	Islet cell hyperplasia
Variation	info
Gene	KCNJ11
CLNDBN	Islet cell hyperplasia
Reversed	1
HGVS	NC_000011.9:g.17409772C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000009209.3,