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: rs12948394
rs12948394
3 17 78386710 intron variant C/T snv 0.47 0.700 1.000 1 2018 2018
dbSNP: rs17561950
rs17561950
4 17 78396063 intron variant G/A snv 0.45 0.700 1.000 1 2018 2018
dbSNP: rs4129767
rs4129767
6 17 78407903 intron variant G/A snv 0.46 0.700 1.000 1 2018 2018
dbSNP: rs4969183
rs4969183
5 17 78397291 intron variant A/G snv 0.46 0.700 1.000 1 2018 2018
dbSNP: rs8071884
rs8071884
4 17 78401977 intron variant C/A;G;T snv 0.700 1.000 1 2019 2019