rs121909616
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs121909616(C;T) |
Make rs121909616(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 154565823 |
Gene | FGB |
is a | snp |
is | mentioned by |
dbSNP | rs121909616 |
dbSNP (classic) | rs121909616 |
ClinGen | rs121909616 |
ebi | rs121909616 |
HLI | rs121909616 |
Exac | rs121909616 |
Gnomad | rs121909616 |
Varsome | rs121909616 |
LitVar | rs121909616 |
Map | rs121909616 |
PheGenI | rs121909616 |
Biobank | rs121909616 |
1000 genomes | rs121909616 |
hgdp | rs121909616 |
ensembl | rs121909616 |
geneview | rs121909616 |
scholar | rs121909616 |
rs121909616 | |
pharmgkb | rs121909616 |
gwascentral | rs121909616 |
openSNP | rs121909616 |
23andMe | rs121909616 |
SNPshot | rs121909616 |
SNPdbe | rs121909616 |
MSV3d | rs121909616 |
GWAS Ctlg | rs121909616 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs121909616(T;T) |
Alt | rs121909616(T;T) |
Reference | Rs121909616(C;C) |
Significance | Other |
Disease | FIBRINOGEN CHRISTCHURCH 2 |
Variation | info |
Gene | FGB |
CLNDBN | FIBRINOGEN CHRISTCHURCH 2 |
Reversed | 0 |
HGVS | NC_000004.11:g.155486975C>T |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000017804.5, |