rs587776561
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(GCTTAGCGTCCTGCGACA;GCTTAGCGTCCTGCGACA) | 0 | common in clinvar |
Make rs587776561(-;-) |
Make rs587776561(-;CTTAGCGTCCTGCGACAG) |
Make rs587776561(CTTAGCGTCCTGCGACAG;CTTAGCGTCCTGCGACAG) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 1 |
Position | 193122213 |
Gene | CDC73, LOC101929160 |
is a | snp |
is | mentioned by |
dbSNP | rs587776561 |
dbSNP (classic) | rs587776561 |
ClinGen | rs587776561 |
ebi | rs587776561 |
HLI | rs587776561 |
Exac | rs587776561 |
Gnomad | rs587776561 |
Varsome | rs587776561 |
LitVar | rs587776561 |
Map | rs587776561 |
PheGenI | rs587776561 |
Biobank | rs587776561 |
1000 genomes | rs587776561 |
hgdp | rs587776561 |
ensembl | rs587776561 |
geneview | rs587776561 |
scholar | rs587776561 |
rs587776561 | |
pharmgkb | rs587776561 |
gwascentral | rs587776561 |
openSNP | rs587776561 |
23andMe | rs587776561 |
SNPshot | rs587776561 |
SNPdbe | rs587776561 |
MSV3d | rs587776561 |
GWAS Ctlg | rs587776561 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587776561(-;-) |
Alt | rs587776561(-;-) |
Reference | Rs587776561(GCTTAGCGTCCTGCGACA;GCTTAGCGTCCTGCGACA) |
Significance | Pathogenic |
Disease | Parathyroid carcinoma |
Variation | info |
Gene | CDC73 LOC101929160 |
CLNDBN | Parathyroid carcinoma |
Reversed | 0 |
HGVS | NC_000001.10:g.193091343_193091360del18 |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000003442.5, |