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: rs2050568
rs2050568
2 0.925 0.160 1 157800451 intron variant C/T snv 0.57 0.700 1.000 1 2011 2011
dbSNP: rs6689427
rs6689427
1 1.000 0.120 1 157811102 intron variant A/G snv 0.44 0.700 1.000 1 2011 2011