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: rs2023843
rs2023843
2 7 27203602 intron variant C/T snv 0.90 0.700 1.000 3 2016 2019
dbSNP: rs4722675
rs4722675
4 7 27204343 intron variant A/G snv 0.93 0.700 1.000 2 2018 2018
dbSNP: rs1859168
rs1859168
13 0.790 0.160 7 27202740 non coding transcript exon variant A/C;G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs2067087
rs2067087
6 1.000 0.080 7 27202041 non coding transcript exon variant G/C;T snv 0.700 1.000 1 2018 2018
dbSNP: rs3735533
rs3735533
4 7 27206274 non coding transcript exon variant T/C snv 0.93 0.700 1.000 1 2016 2016
dbSNP: rs60772526
rs60772526
1 7 27206377 non coding transcript exon variant C/G;T snv 0.700 1.000 1 2019 2019