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: rs1007392
rs1007392
2 11 14753045 intron variant A/G snv 0.35 0.700 1.000 1 2014 2014
dbSNP: rs11023332
rs11023332
2 11 14762564 intron variant G/C snv 0.35 0.700 1.000 1 2014 2014
dbSNP: rs116970203
rs116970203
2 11 14855172 intron variant G/A snv 2.2E-02 0.700 1.000 1 2017 2017