rs199469508
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs199469508(C;C) |
Make rs199469508(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 173917217 |
Gene | SERPINC1 |
is a | snp |
is | mentioned by |
dbSNP | rs199469508 |
dbSNP (classic) | rs199469508 |
ClinGen | rs199469508 |
ebi | rs199469508 |
HLI | rs199469508 |
Exac | rs199469508 |
Gnomad | rs199469508 |
Varsome | rs199469508 |
LitVar | rs199469508 |
Map | rs199469508 |
PheGenI | rs199469508 |
Biobank | rs199469508 |
1000 genomes | rs199469508 |
hgdp | rs199469508 |
ensembl | rs199469508 |
geneview | rs199469508 |
scholar | rs199469508 |
rs199469508 | |
pharmgkb | rs199469508 |
gwascentral | rs199469508 |
openSNP | rs199469508 |
23andMe | rs199469508 |
SNPshot | rs199469508 |
SNPdbe | rs199469508 |
MSV3d | rs199469508 |
GWAS Ctlg | rs199469508 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs199469508(C;C) |
Alt | rs199469508(C;C) |
Reference | Rs199469508(T;T) |
Significance | Untested |
Disease | |
Variation | info |
Gene | SERPINC1 |
CLNDBN | OMIM |
Reversed | 1 |
HGVS | NC_000001.10:g.173886355A>G |
CLNSRC | |
CLNACC |