rs587776841
From SNPedia
Orientation | plus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(-;GTCT) | 5.8 | Multiple Endocrine Neoplasia Type 1 |
(AGAC;AGAC) | 0 | common in clinvar |
(GTCT;GTCT) | 0 | common in clinvar |
(I;I) | 0 | common genotype |
Make rs587776841(-;-) |
Make rs587776841(-;AGAC) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 11 |
Position | 64809858 |
Gene | MEN1 |
is a | snp |
is | mentioned by |
dbSNP | rs587776841 |
dbSNP (classic) | rs587776841 |
ClinGen | rs587776841 |
ebi | rs587776841 |
HLI | rs587776841 |
Exac | rs587776841 |
Gnomad | rs587776841 |
Varsome | rs587776841 |
LitVar | rs587776841 |
Map | rs587776841 |
PheGenI | rs587776841 |
Biobank | rs587776841 |
1000 genomes | rs587776841 |
hgdp | rs587776841 |
ensembl | rs587776841 |
geneview | rs587776841 |
scholar | rs587776841 |
rs587776841 | |
pharmgkb | rs587776841 |
gwascentral | rs587776841 |
openSNP | rs587776841 |
23andMe | rs587776841 |
SNPshot | rs587776841 |
SNPdbe | rs587776841 |
MSV3d | rs587776841 |
GWAS Ctlg | rs587776841 |
Max Magnitude | 5.8 |
ClinVar | |
---|---|
Risk | Rs587776841(AGAC;AGAC) rs587776841(-;-) |
Alt | Rs587776841(AGAC;AGAC) rs587776841(-;-) |
Reference | Rs587776841(GTCT;GTCT) |
Significance | Pathogenic |
Disease | Lipoma not provided Multiple endocrine neoplasia Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | MEN1 |
CLNDBN | Lipoma, somatic not provided Multiple endocrine neoplasia, type 1 Hereditary cancer-predisposing syndrome |
Reversed | 1 |
HGVS | NC_000011.9:g.64577330_64577333delAGAC |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000018173.4, RCV000182434.2, RCV000206170.3, RCV000491114.1, |