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: rs2688482
rs2688482
1 1.000 0.120 3 195802247 intron variant T/C snv 0.66 0.700 1.000 1 2015 2015
dbSNP: rs3103933
rs3103933
1 1.000 0.120 3 195758569 intron variant A/G;T snv 0.700 1.000 1 2015 2015