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: rs2653570
rs2653570
1 11 8966276 intron variant A/G snv 0.54 0.700 1.000 1 2012 2012
dbSNP: rs2742480
rs2742480
1 11 8971583 intron variant A/G snv 0.54 0.700 1.000 1 2012 2012