rs267607196

Orientation

minus

Stabilized

minus

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

Make rs267607196(A;A)

Make rs267607196(A;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

17387248

Gene

KCNJ11

is a	snp
is	mentioned by
dbSNP	rs267607196
dbSNP (classic)	rs267607196
ClinGen	rs267607196
ebi	rs267607196
HLI	rs267607196
Exac	rs267607196
Gnomad	rs267607196
Varsome	rs267607196
LitVar	rs267607196
Map	rs267607196
PheGenI	rs267607196
Biobank	rs267607196
1000 genomes	rs267607196
hgdp	rs267607196
ensembl	rs267607196
geneview	rs267607196
scholar	rs267607196
google	rs267607196
pharmgkb	rs267607196
gwascentral	rs267607196
openSNP	rs267607196
23andMe	rs267607196
SNPshot	rs267607196
SNPdbe	rs267607196
MSV3d	rs267607196
GWAS Ctlg	rs267607196

Max Magnitude

0

ClinVar
Risk	rs267607196(A;A)
Alt	rs267607196(A;A)
Reference	Rs267607196(G;G)
Significance	Pathogenic
Disease	Islet cell hyperplasia
Variation	info
Gene	KCNJ11
CLNDBN	Islet cell hyperplasia
Reversed	1
HGVS	NC_000011.9:g.17408795C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000009223.5,