rs199469487
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(GCTTTCAA;GCTTTCAA) | 0 | common in clinvar |
Make rs199469487(GCTTTCAA;TGAAAGC) |
Make rs199469487(TGAAAGC;TGAAAGC) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 93905802 |
Gene | PROS1 |
is a | snp |
is | mentioned by |
dbSNP | rs199469487 |
dbSNP (classic) | rs199469487 |
ClinGen | rs199469487 |
ebi | rs199469487 |
HLI | rs199469487 |
Exac | rs199469487 |
Gnomad | rs199469487 |
Varsome | rs199469487 |
LitVar | rs199469487 |
Map | rs199469487 |
PheGenI | rs199469487 |
Biobank | rs199469487 |
1000 genomes | rs199469487 |
hgdp | rs199469487 |
ensembl | rs199469487 |
geneview | rs199469487 |
scholar | rs199469487 |
rs199469487 | |
pharmgkb | rs199469487 |
gwascentral | rs199469487 |
openSNP | rs199469487 |
23andMe | rs199469487 |
SNPshot | rs199469487 |
SNPdbe | rs199469487 |
MSV3d | rs199469487 |
GWAS Ctlg | rs199469487 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs199469487(TGAAAGC;TGAAAGC) |
Alt | rs199469487(TGAAAGC;TGAAAGC) |
Reference | Rs199469487(GCTTTCAA;GCTTTCAA) |
Significance | Untested |
Disease | |
Variation | info |
Gene | PROS1 |
CLNDBN | OMIM |
Reversed | 1 |
HGVS | NC_000003.11:g.93624646_93624653delTTGAAAGCinsGCTTTCA |
CLNSRC | |
CLNACC |