rs786202253
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(GCTTCAAA;GCTTCAAA) | 0 | common in clinvar |
Make rs786202253(-;-) |
Make rs786202253(-;GCTTCAAA) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 11 |
Position | 94478768 |
Gene | MRE11A |
is a | snp |
is | mentioned by |
dbSNP | rs786202253 |
dbSNP (classic) | rs786202253 |
ClinGen | rs786202253 |
ebi | rs786202253 |
HLI | rs786202253 |
Exac | rs786202253 |
Gnomad | rs786202253 |
Varsome | rs786202253 |
LitVar | rs786202253 |
Map | rs786202253 |
PheGenI | rs786202253 |
Biobank | rs786202253 |
1000 genomes | rs786202253 |
hgdp | rs786202253 |
ensembl | rs786202253 |
geneview | rs786202253 |
scholar | rs786202253 |
rs786202253 | |
pharmgkb | rs786202253 |
gwascentral | rs786202253 |
openSNP | rs786202253 |
23andMe | rs786202253 |
SNPshot | rs786202253 |
SNPdbe | rs786202253 |
MSV3d | rs786202253 |
GWAS Ctlg | rs786202253 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs786202253(-;-) |
Alt | rs786202253(-;-) |
Reference | Rs786202253(GCTTCAAA;GCTTCAAA) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | MRE11A |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 1 |
HGVS | NC_000011.9:g.94211934_94211941delTTTGAAGC |
CLNSRC | |
CLNACC | RCV000164971.2, |