rs10485275, GRIK2

N. diseases: 1
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.
Miscarriage
CUI: C4552766
Disease: Miscarriage
56 1.000 0.040 6 101718178 intron variant G/A;T snv 0.010 1.000 1 2011 2011