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: rs10998461
rs10998461
1 1.000 0.080 10 68856761 intron variant G/T snv 0.44 0.010 1.000 1 2020 2020
dbSNP: rs10998468
rs10998468
1 1.000 0.080 10 68867495 intron variant T/C snv 0.22 0.010 1.000 1 2020 2020
dbSNP: rs4472827
rs4472827
1 1.000 0.080 10 68892516 intron variant G/A snv 0.33 0.010 1.000 1 2020 2020
dbSNP: rs7903209
rs7903209
1 1.000 0.080 10 68868826 intron variant C/T snv 0.28 0.010 1.000 1 2020 2020