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: rs971681
rs971681
1 14 29605481 intron variant C/T snv 0.43 0.700 1.000 2 2018 2019
dbSNP: rs1959440
rs1959440
2 1.000 0.040 14 29739424 intron variant G/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs2068012
rs2068012
2 1.000 0.040 14 29721110 intron variant T/C snv 0.28 0.700 1.000 1 2019 2019
dbSNP: rs2333604
rs2333604
1 14 29602532 intron variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs28645341
rs28645341
1 14 29704872 intron variant T/C snv 0.32 0.700 1.000 1 2018 2018