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: rs11630479
rs11630479
1 15 98697252 intron variant G/A snv 0.39 0.700 1.000 1 2019 2019
dbSNP: rs7402982
rs7402982
1 15 98650040 intron variant A/G snv 0.63 0.700 1.000 1 2016 2016
dbSNP: rs7402983
rs7402983
1 15 98650047 intron variant A/C snv 0.65 0.700 1.000 1 2019 2019