rs1057520672
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs1057520672(C;T) |
Make rs1057520672(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 11 |
Position | 108347335 |
Gene | ATM, C11orf65 |
is a | snp |
is | mentioned by |
dbSNP | rs1057520672 |
dbSNP (classic) | rs1057520672 |
ClinGen | rs1057520672 |
ebi | rs1057520672 |
HLI | rs1057520672 |
Exac | rs1057520672 |
Gnomad | rs1057520672 |
Varsome | rs1057520672 |
LitVar | rs1057520672 |
Map | rs1057520672 |
PheGenI | rs1057520672 |
Biobank | rs1057520672 |
1000 genomes | rs1057520672 |
hgdp | rs1057520672 |
ensembl | rs1057520672 |
geneview | rs1057520672 |
scholar | rs1057520672 |
rs1057520672 | |
pharmgkb | rs1057520672 |
gwascentral | rs1057520672 |
openSNP | rs1057520672 |
23andMe | rs1057520672 |
SNPshot | rs1057520672 |
SNPdbe | rs1057520672 |
MSV3d | rs1057520672 |
GWAS Ctlg | rs1057520672 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1057520672(T;T) |
Alt | rs1057520672(T;T) |
Reference | Rs1057520672(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | C11orf65 ATM |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000011.9:g.108218062C>T |
CLNSRC | |
CLNACC | RCV000421983.1, |