rs775522201
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs775522201(C;T) |
Make rs775522201(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 8 |
Position | 127738393 |
Gene | MYC |
is a | snp |
is | mentioned by |
dbSNP | rs775522201 |
dbSNP (classic) | rs775522201 |
ClinGen | rs775522201 |
ebi | rs775522201 |
HLI | rs775522201 |
Exac | rs775522201 |
Gnomad | rs775522201 |
Varsome | rs775522201 |
LitVar | rs775522201 |
Map | rs775522201 |
PheGenI | rs775522201 |
Biobank | rs775522201 |
1000 genomes | rs775522201 |
hgdp | rs775522201 |
ensembl | rs775522201 |
geneview | rs775522201 |
scholar | rs775522201 |
rs775522201 | |
pharmgkb | rs775522201 |
gwascentral | rs775522201 |
openSNP | rs775522201 |
23andMe | rs775522201 |
SNPshot | rs775522201 |
SNPdbe | rs775522201 |
MSV3d | rs775522201 |
GWAS Ctlg | rs775522201 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs775522201(T;T) |
Alt | rs775522201(T;T) |
Reference | Rs775522201(C;C) |
Significance | Probable-Pathogenic |
Disease | Neoplasm |
Variation | info |
Gene | MYC |
CLNDBN | Neoplasm |
Reversed | 0 |
HGVS | NC_000008.10:g.128750639C>T |
CLNSRC | |
CLNACC | RCV000440255.1, |