rs398124437
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;G) | 5.8 | Multiple Endocrine Neoplasia Type 1 |
(G;G) | 0 | common in clinvar |
Make rs398124437(A;A) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 64807010 |
Gene | MEN1 |
is a | snp |
is | mentioned by |
dbSNP | rs398124437 |
dbSNP (classic) | rs398124437 |
ClinGen | rs398124437 |
ebi | rs398124437 |
HLI | rs398124437 |
Exac | rs398124437 |
Gnomad | rs398124437 |
Varsome | rs398124437 |
LitVar | rs398124437 |
Map | rs398124437 |
PheGenI | rs398124437 |
Biobank | rs398124437 |
1000 genomes | rs398124437 |
hgdp | rs398124437 |
ensembl | rs398124437 |
geneview | rs398124437 |
scholar | rs398124437 |
rs398124437 | |
pharmgkb | rs398124437 |
gwascentral | rs398124437 |
openSNP | rs398124437 |
23andMe | rs398124437 |
SNPshot | rs398124437 |
SNPdbe | rs398124437 |
MSV3d | rs398124437 |
GWAS Ctlg | rs398124437 |
Max Magnitude | 5.8 |
ClinVar | |
---|---|
Risk | rs398124437(A;A) rs398124437(C;C) |
Alt | rs398124437(A;A) rs398124437(C;C) |
Reference | Rs398124437(G;G) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome not provided |
Variation | info |
Gene | MEN1 |
CLNDBN | Hereditary cancer-predisposing syndrome not provided |
Reversed | 1 |
HGVS | NC_000011.9:g.64574482C>G; NC_000011.9:g.64574482C>T |
CLNSRC | HGMD |
CLNACC | RCV000490972.1, RCV000082339.6, RCV000491428.1, |