rs387906783
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs387906783(A;A) |
Make rs387906783(A;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 17387913 |
Gene | KCNJ11 |
is a | snp |
is | mentioned by |
dbSNP | rs387906783 |
dbSNP (classic) | rs387906783 |
ClinGen | rs387906783 |
ebi | rs387906783 |
HLI | rs387906783 |
Exac | rs387906783 |
Gnomad | rs387906783 |
Varsome | rs387906783 |
LitVar | rs387906783 |
Map | rs387906783 |
PheGenI | rs387906783 |
Biobank | rs387906783 |
1000 genomes | rs387906783 |
hgdp | rs387906783 |
ensembl | rs387906783 |
geneview | rs387906783 |
scholar | rs387906783 |
rs387906783 | |
pharmgkb | rs387906783 |
gwascentral | rs387906783 |
openSNP | rs387906783 |
23andMe | rs387906783 |
SNPshot | rs387906783 |
SNPdbe | rs387906783 |
MSV3d | rs387906783 |
GWAS Ctlg | rs387906783 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs387906783(A;A) |
Alt | rs387906783(A;A) |
Reference | Rs387906783(T;T) |
Significance | Pathogenic |
Disease | Diabetes mellitus |
Variation | info |
Gene | KCNJ11 |
CLNDBN | Diabetes mellitus, permanent neonatal, with neurologic features |
Reversed | 1 |
HGVS | NC_000011.9:g.17409460A>T |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000023046.4, |