rs104894236

Orientation

minus

Stabilized

minus

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

Make rs104894236(A;A)

Make rs104894236(A;C)

Reference

GRCh38 38.1/141

Chromosome

11

Position

17388056

Gene

KCNJ11

is a	snp
is	mentioned by
dbSNP	rs104894236
dbSNP (classic)	rs104894236
ClinGen	rs104894236
ebi	rs104894236
HLI	rs104894236
Exac	rs104894236
Gnomad	rs104894236
Varsome	rs104894236
LitVar	rs104894236
Map	rs104894236
PheGenI	rs104894236
Biobank	rs104894236
1000 genomes	rs104894236
hgdp	rs104894236
ensembl	rs104894236
geneview	rs104894236
scholar	rs104894236
google	rs104894236
pharmgkb	rs104894236
gwascentral	rs104894236
openSNP	rs104894236
23andMe	rs104894236
SNPshot	rs104894236
SNPdbe	rs104894236
MSV3d	rs104894236
GWAS Ctlg	rs104894236

Max Magnitude

0

OMIM	600937
Desc
Variant	0009
Related	also

ClinVar
Risk	rs104894236(A;A) rs104894236(T;T)
Alt	rs104894236(A;A) rs104894236(T;T)
Reference	Rs104894236(C;C)
Significance	Pathogenic
Disease	Islet cell hyperplasia
Variation	info
Gene	KCNJ11
CLNDBN	Islet cell hyperplasia
Reversed	1
HGVS	NC_000011.9:g.17409603G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000009208.3,