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: rs1142
rs1142
6 0.851 0.040 7 105115879 intron variant C/T snv 0.31 0.700 1.000 1 2019 2019
dbSNP: rs1144
rs1144
2 7 105115908 intron variant T/C snv 0.31 0.700 1.000 1 2018 2018
dbSNP: rs2057884
rs2057884
2 1.000 0.040 7 105289803 intron variant T/C snv 0.59 0.700 1.000 1 2019 2019
dbSNP: rs4730073
rs4730073
1 7 105215424 intron variant C/A;T snv 0.700 1.000 1 2019 2019