rs202100019
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs202100019(C;T) |
Make rs202100019(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 2 |
Position | 73850446 |
Gene | LOC105374806, STAMBP |
is a | snp |
is | mentioned by |
dbSNP | rs202100019 |
dbSNP (classic) | rs202100019 |
ClinGen | rs202100019 |
ebi | rs202100019 |
HLI | rs202100019 |
Exac | rs202100019 |
Gnomad | rs202100019 |
Varsome | rs202100019 |
LitVar | rs202100019 |
Map | rs202100019 |
PheGenI | rs202100019 |
Biobank | rs202100019 |
1000 genomes | rs202100019 |
hgdp | rs202100019 |
ensembl | rs202100019 |
geneview | rs202100019 |
scholar | rs202100019 |
rs202100019 | |
pharmgkb | rs202100019 |
gwascentral | rs202100019 |
openSNP | rs202100019 |
23andMe | rs202100019 |
SNPshot | rs202100019 |
SNPdbe | rs202100019 |
MSV3d | rs202100019 |
GWAS Ctlg | rs202100019 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs202100019(T;T) |
Alt | rs202100019(T;T) |
Reference | Rs202100019(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | STAMBP |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.74077573C>T |
CLNSRC | |
CLNACC | RCV000487330.1, |