rs869312167
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs869312167(-;-) |
Make rs869312167(-;A) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 11 |
Position | 64809958 |
Gene | MEN1 |
is a | snp |
is | mentioned by |
dbSNP | rs869312167 |
dbSNP (classic) | rs869312167 |
ClinGen | rs869312167 |
ebi | rs869312167 |
HLI | rs869312167 |
Exac | rs869312167 |
Gnomad | rs869312167 |
Varsome | rs869312167 |
LitVar | rs869312167 |
Map | rs869312167 |
PheGenI | rs869312167 |
Biobank | rs869312167 |
1000 genomes | rs869312167 |
hgdp | rs869312167 |
ensembl | rs869312167 |
geneview | rs869312167 |
scholar | rs869312167 |
rs869312167 | |
pharmgkb | rs869312167 |
gwascentral | rs869312167 |
openSNP | rs869312167 |
23andMe | rs869312167 |
SNPshot | rs869312167 |
SNPdbe | rs869312167 |
MSV3d | rs869312167 |
GWAS Ctlg | rs869312167 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs869312167(-;-) |
Alt | rs869312167(-;-) |
Reference | Rs869312167(A;A) |
Significance | Pathogenic |
Disease | Primary hyperparathyroidism |
Variation | info |
Gene | MEN1 |
CLNDBN | Primary hyperparathyroidism |
Reversed | 1 |
HGVS | NC_000011.9:g.64577430delT |
CLNSRC | |
CLNACC | RCV000210355.1, |