Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs757978
rs757978
FARP2
0.851 0.200 2 241431686 missense variant C/A;T snv 4.1E-06; 9.3E-02
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia 		0.820 1.000 2 2010 2013
dbSNP: rs1476698
rs1476698
FARP2
2 241357034 intron variant A/G;T snv
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay 		0.800 1.000 1 2013 2017
dbSNP: rs1476698
rs1476698
FARP2
2 241357034 intron variant A/G;T snv
CUI: C1325327
Disease: fibrinogen activity
fibrinogen activity 		0.700 1.000 1 2013 2013
dbSNP: rs1476698
rs1476698
FARP2
2 241357034 intron variant A/G;T snv
CUI: C1561955
Disease: Fibrinogen, CTCAE
Fibrinogen, CTCAE 		0.700 1.000 1 2013 2013
dbSNP: rs3771570
rs3771570
FARP2
0.925 0.080 2 241443449 3 prime UTR variant C/T snv 0.11
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.700 1.000 1 2013 2013
dbSNP: rs757978
rs757978
FARP2
0.851 0.200 2 241431686 missense variant C/A;T snv 4.1E-06; 9.3E-02
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma 		0.700 1.000 1 2010 2010