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: rs1290784
rs1290784
6 3 169379112 intron variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs1290786
rs1290786
1 3 169379593 intron variant C/T snv 0.42 0.700 1.000 1 2018 2018
dbSNP: rs1918973
rs1918973
2 3 169447385 intron variant A/G snv 0.57 0.700 1.000 1 2018 2018
dbSNP: rs419076
rs419076
6 3 169383098 intron variant T/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs448378
rs448378
5 1.000 0.040 3 169383111 intron variant G/A;C snv 0.700 1.000 1 2016 2016
dbSNP: rs988398
rs988398
3 3 169381073 intron variant C/T snv 0.45 0.700 1.000 1 2018 2018