rs199731535
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs199731535(A;A) |
Make rs199731535(A;C) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 3 |
Position | 142549478 |
Gene | ATR |
is a | snp |
is | mentioned by |
dbSNP | rs199731535 |
dbSNP (classic) | rs199731535 |
ClinGen | rs199731535 |
ebi | rs199731535 |
HLI | rs199731535 |
Exac | rs199731535 |
Gnomad | rs199731535 |
Varsome | rs199731535 |
LitVar | rs199731535 |
Map | rs199731535 |
PheGenI | rs199731535 |
Biobank | rs199731535 |
1000 genomes | rs199731535 |
hgdp | rs199731535 |
ensembl | rs199731535 |
geneview | rs199731535 |
scholar | rs199731535 |
rs199731535 | |
pharmgkb | rs199731535 |
gwascentral | rs199731535 |
openSNP | rs199731535 |
23andMe | rs199731535 |
SNPshot | rs199731535 |
SNPdbe | rs199731535 |
MSV3d | rs199731535 |
GWAS Ctlg | rs199731535 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs199731535(A;A) rs199731535(T;T) |
Alt | rs199731535(A;A) rs199731535(T;T) |
Reference | Rs199731535(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | ATR |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000003.11:g.142268320C>T |
CLNSRC | |
CLNACC | RCV000434115.1, |