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: rs2241208
rs2241208
2 12 109524990 intron variant G/C snv 0.57 0.700 1.000 3 2015 2019
dbSNP: rs10744826
rs10744826
3 12 109527707 intron variant C/G snv 0.57 0.700 1.000 2 2018 2019
dbSNP: rs2241210
rs2241210
1 12 109512339 intron variant A/G snv 0.57 0.700 1.000 2 2017 2019