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: rs11136775
rs11136775
2 0.925 0.040 8 4791194 intron variant G/C snv 0.12 0.700 1.000 1 2018 2018
dbSNP: rs11787412
rs11787412
2 0.925 0.040 8 3276717 intron variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs13260434
rs13260434
2 0.925 0.040 8 3368702 intron variant T/A snv 0.24 0.700 1.000 1 2018 2018