rs879255609
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs879255609(-;-) |
Make rs879255609(-;G) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 9 |
Position | 4118546 |
Gene | GLIS3 |
is a | snp |
is | mentioned by |
dbSNP | rs879255609 |
dbSNP (classic) | rs879255609 |
ClinGen | rs879255609 |
ebi | rs879255609 |
HLI | rs879255609 |
Exac | rs879255609 |
Gnomad | rs879255609 |
Varsome | rs879255609 |
LitVar | rs879255609 |
Map | rs879255609 |
PheGenI | rs879255609 |
Biobank | rs879255609 |
1000 genomes | rs879255609 |
hgdp | rs879255609 |
ensembl | rs879255609 |
geneview | rs879255609 |
scholar | rs879255609 |
rs879255609 | |
pharmgkb | rs879255609 |
gwascentral | rs879255609 |
openSNP | rs879255609 |
23andMe | rs879255609 |
SNPshot | rs879255609 |
SNPdbe | rs879255609 |
MSV3d | rs879255609 |
GWAS Ctlg | rs879255609 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs879255609(-;-) |
Alt | rs879255609(-;-) |
Reference | Rs879255609(G;G) |
Significance | Pathogenic |
Disease | Diabetes mellitus |
Variation | info |
Gene | GLIS3 |
CLNDBN | Diabetes mellitus, neonatal, with congenital hypothyroidism |
Reversed | 1 |
HGVS | NC_000009.11:g.4118546delC |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000239491.1, |