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: rs4981022
rs4981022
2 12 103756096 intron variant G/A snv 0.69 0.700 1.000 3 2010 2019
dbSNP: rs1070073
rs1070073
2 12 103606541 intron variant T/G snv 0.71 0.700 1.000 1 2019 2019
dbSNP: rs11111679
rs11111679
1 12 103613640 intron variant G/A snv 5.5E-02 0.700 1.000 1 2019 2019
dbSNP: rs73192004
rs73192004
1 12 103733575 intron variant G/A snv 3.9E-02 0.700 1.000 1 2019 2019