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: rs845084
rs845084
2 1.000 0.040 10 123460520 intron variant G/A snv 0.26 0.700 1.000 2 2019 2019
dbSNP: rs1568079
rs1568079
1 10 123492235 intron variant T/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs7090367
rs7090367
1 10 123474976 intron variant T/C snv 0.38 0.700 1.000 1 2017 2017