rs876658770
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs876658770(C;T) |
Make rs876658770(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 5 |
Position | 132640768 |
Gene | RAD50, TH2LCRR |
is a | snp |
is | mentioned by |
dbSNP | rs876658770 |
dbSNP (classic) | rs876658770 |
ClinGen | rs876658770 |
ebi | rs876658770 |
HLI | rs876658770 |
Exac | rs876658770 |
Gnomad | rs876658770 |
Varsome | rs876658770 |
LitVar | rs876658770 |
Map | rs876658770 |
PheGenI | rs876658770 |
Biobank | rs876658770 |
1000 genomes | rs876658770 |
hgdp | rs876658770 |
ensembl | rs876658770 |
geneview | rs876658770 |
scholar | rs876658770 |
rs876658770 | |
pharmgkb | rs876658770 |
gwascentral | rs876658770 |
openSNP | rs876658770 |
23andMe | rs876658770 |
SNPshot | rs876658770 |
SNPdbe | rs876658770 |
MSV3d | rs876658770 |
GWAS Ctlg | rs876658770 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs876658770(T;T) |
Alt | rs876658770(T;T) |
Reference | Rs876658770(C;C) |
Significance | Other |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | LOC101927761 TH2LCRR RAD50 |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000005.9:g.131976460C>T |
CLNSRC | |
CLNACC | RCV000222314.1, |