rs868197660
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs868197660(A;A) |
Make rs868197660(A;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 9 |
Position | 4117797 |
Gene | GLIS3 |
is a | snp |
is | mentioned by |
dbSNP | rs868197660 |
dbSNP (classic) | rs868197660 |
ClinGen | rs868197660 |
ebi | rs868197660 |
HLI | rs868197660 |
Exac | rs868197660 |
Gnomad | rs868197660 |
Varsome | rs868197660 |
LitVar | rs868197660 |
Map | rs868197660 |
PheGenI | rs868197660 |
Biobank | rs868197660 |
1000 genomes | rs868197660 |
hgdp | rs868197660 |
ensembl | rs868197660 |
geneview | rs868197660 |
scholar | rs868197660 |
rs868197660 | |
pharmgkb | rs868197660 |
gwascentral | rs868197660 |
openSNP | rs868197660 |
23andMe | rs868197660 |
SNPshot | rs868197660 |
SNPdbe | rs868197660 |
MSV3d | rs868197660 |
GWAS Ctlg | rs868197660 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs868197660(A;A) |
Alt | rs868197660(A;A) |
Reference | Rs868197660(G;G) |
Significance | Pathogenic |
Disease | Diabetes mellitus |
Variation | info |
Gene | GLIS3 |
CLNDBN | Diabetes mellitus, neonatal, with congenital hypothyroidism |
Reversed | 0 |
HGVS | NC_000009.11:g.4117797G>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000239596.1, |