rs1060500020
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs1060500020(-;-) |
Make rs1060500020(-;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 1 |
Position | 193122204 |
Gene | CDC73, LOC101929160 |
is a | snp |
is | mentioned by |
dbSNP | rs1060500020 |
dbSNP (classic) | rs1060500020 |
ClinGen | rs1060500020 |
ebi | rs1060500020 |
HLI | rs1060500020 |
Exac | rs1060500020 |
Gnomad | rs1060500020 |
Varsome | rs1060500020 |
LitVar | rs1060500020 |
Map | rs1060500020 |
PheGenI | rs1060500020 |
Biobank | rs1060500020 |
1000 genomes | rs1060500020 |
hgdp | rs1060500020 |
ensembl | rs1060500020 |
geneview | rs1060500020 |
scholar | rs1060500020 |
rs1060500020 | |
pharmgkb | rs1060500020 |
gwascentral | rs1060500020 |
openSNP | rs1060500020 |
23andMe | rs1060500020 |
SNPshot | rs1060500020 |
SNPdbe | rs1060500020 |
MSV3d | rs1060500020 |
GWAS Ctlg | rs1060500020 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1060500020(-;-) |
Alt | rs1060500020(-;-) |
Reference | Rs1060500020(G;G) |
Significance | Pathogenic |
Disease | Parathyroid carcinoma |
Variation | info |
Gene | CDC73 LOC101929160 |
CLNDBN | Parathyroid carcinoma |
Reversed | 0 |
HGVS | NC_000001.10:g.193091334delG |
CLNSRC | |
CLNACC | RCV000463923.1, |