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: rs1476098
rs1476098
1 1.000 0.040 17 61159652 intron variant A/C snv 0.66 0.700 1.000 1 2018 2018
dbSNP: rs7212798
rs7212798
1 1.000 0.040 17 60936127 intron variant T/A;C snv 0.700 1.000 1 2015 2015
dbSNP: rs8068952
rs8068952
2 1.000 0.040 17 61209283 intron variant G/C snv 0.60 0.700 1.000 1 2017 2017
dbSNP: rs8079951
rs8079951
1 1.000 0.040 17 61165403 intron variant T/A snv 0.68 0.700 1.000 1 2018 2018
dbSNP: rs8080784
rs8080784
1 1.000 0.040 17 60939664 intron variant T/C snv 0.22 0.700 1.000 1 2018 2018