rs1369837875, PLA2G6

N. diseases: 4
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Factor V Leiden mutation
CUI: C0584960
Disease: Factor V Leiden mutation
46 0.882 0.200 22 38128276 synonymous variant G/A snv 0.010 1.000 1 2005 2005
Miscarriage
CUI: C4552766
Disease: Miscarriage
56 0.882 0.200 22 38128276 synonymous variant G/A snv 0.010 1.000 1 2017 2017
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.882 0.200 22 38128276 synonymous variant G/A snv 0.010 1.000 1 2002 2002
Polyendocrinopathies, Autoimmune
CUI: C0085409
Disease: Polyendocrinopathies, Autoimmune
21 0.882 0.200 22 38128276 synonymous variant G/A snv 0.010 1.000 1 2008 2008