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: rs11858316
rs11858316
3 0.925 0.120 15 98705800 intron variant C/T snv 0.50 0.700 1.000 1 2019 2019
dbSNP: rs143193096
rs143193096
3 15 98916098 missense variant G/A;C snv 8.4E-05; 4.0E-06 0.700 1.000 1 2018 2018
dbSNP: rs2137683
rs2137683
3 0.925 0.120 15 98746409 intron variant C/G snv 0.53 0.700 1.000 1 2019 2019
dbSNP: rs4966025
rs4966025
1 15 98766313 intron variant G/A snv 0.60 0.700 1.000 1 2018 2018
dbSNP: rs59646751
rs59646751
1 15 98733292 intron variant G/T snv 0.31 0.700 1.000 1 2019 2019