rs199469492
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs199469492(G;T) |
Make rs199469492(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 93892933 |
Gene | PROS1 |
is a | snp |
is | mentioned by |
dbSNP | rs199469492 |
dbSNP (classic) | rs199469492 |
ClinGen | rs199469492 |
ebi | rs199469492 |
HLI | rs199469492 |
Exac | rs199469492 |
Gnomad | rs199469492 |
Varsome | rs199469492 |
LitVar | rs199469492 |
Map | rs199469492 |
PheGenI | rs199469492 |
Biobank | rs199469492 |
1000 genomes | rs199469492 |
hgdp | rs199469492 |
ensembl | rs199469492 |
geneview | rs199469492 |
scholar | rs199469492 |
rs199469492 | |
pharmgkb | rs199469492 |
gwascentral | rs199469492 |
openSNP | rs199469492 |
23andMe | rs199469492 |
SNPshot | rs199469492 |
SNPdbe | rs199469492 |
MSV3d | rs199469492 |
GWAS Ctlg | rs199469492 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs199469492(T;T) |
Alt | rs199469492(T;T) |
Reference | Rs199469492(G;G) |
Significance | Untested |
Disease | |
Variation | info |
Gene | PROS1 |
CLNDBN | OMIM |
Reversed | 1 |
HGVS | NC_000003.11:g.93611777C>A |
CLNSRC | |
CLNACC |