rs104894237

Orientation

minus

Stabilized

minus

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

Make rs104894237(C;T)

Make rs104894237(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

17387331

Gene

KCNJ11

is a	snp
is	mentioned by
dbSNP	rs104894237
dbSNP (classic)	rs104894237
ClinGen	rs104894237
ebi	rs104894237
HLI	rs104894237
Exac	rs104894237
Gnomad	rs104894237
Varsome	rs104894237
LitVar	rs104894237
Map	rs104894237
PheGenI	rs104894237
Biobank	rs104894237
1000 genomes	rs104894237
hgdp	rs104894237
ensembl	rs104894237
geneview	rs104894237
scholar	rs104894237
google	rs104894237
pharmgkb	rs104894237
gwascentral	rs104894237
openSNP	rs104894237
23andMe	rs104894237
SNPshot	rs104894237
SNPdbe	rs104894237
MSV3d	rs104894237
GWAS Ctlg	rs104894237

Max Magnitude

0

OMIM	600937
Desc
Variant	0011
Related	also

ClinVar
Risk	rs104894237(T;T)
Alt	rs104894237(T;T)
Reference	Rs104894237(C;C)
Significance	Pathogenic
Disease	Islet cell hyperplasia
Variation	info
Gene	KCNJ11
CLNDBN	Islet cell hyperplasia
Reversed	1
HGVS	NC_000011.9:g.17408878G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000009210.3,