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: rs7650482
rs7650482
1 1.000 0.080 3 12800305 intron variant A/G snv 0.68 0.700 1.000 2 2018 2018
dbSNP: rs6810325
rs6810325
2 1.000 0.080 3 12799435 intron variant T/C snv 0.66 0.700 1.000 1 2018 2018
dbSNP: rs4642101
rs4642101
3 1.000 0.080 3 12800724 intron variant T/G snv 0.63 0.020 1.000 2 2016 2018