rs121918486
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs121918486(C;G) |
Make rs121918486(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 46739324 |
Gene | F2 |
is a | snp |
is | mentioned by |
dbSNP | rs121918486 |
dbSNP (classic) | rs121918486 |
ClinGen | rs121918486 |
ebi | rs121918486 |
HLI | rs121918486 |
Exac | rs121918486 |
Gnomad | rs121918486 |
Varsome | rs121918486 |
LitVar | rs121918486 |
Map | rs121918486 |
PheGenI | rs121918486 |
Biobank | rs121918486 |
1000 genomes | rs121918486 |
hgdp | rs121918486 |
ensembl | rs121918486 |
geneview | rs121918486 |
scholar | rs121918486 |
rs121918486 | |
pharmgkb | rs121918486 |
gwascentral | rs121918486 |
openSNP | rs121918486 |
23andMe | rs121918486 |
SNPshot | rs121918486 |
SNPdbe | rs121918486 |
MSV3d | rs121918486 |
GWAS Ctlg | rs121918486 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs121918486(G;G) |
Alt | rs121918486(G;G) |
Reference | Rs121918486(C;C) |
Significance | Pathogenic |
Disease | Hereditary factor II deficiency disease |
Variation | info |
Gene | F2 |
CLNDBN | Hereditary factor II deficiency disease |
Reversed | 0 |
HGVS | NC_000011.9:g.46760874C>G |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000014242.18, |