PRF1, perforin 1, 5551

N. diseases: 163; N. variants: 31
Disease: Hypofibrinogenemia ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs768849283
rs768849283
Entrez Id: 5551
Gene Symbol: PRF1
PRF1
CUI: C0553681
Disease:
Hypofibrinogenemia 		G 0.700 GeneticVariation CLINVAR