Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2227281
rs2227281
GRIK2
1 1.000 0.040 6 102055321 intron variant C/T snv 0.31 0.29 0.010 1.000 1 2007 2007