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: rs13337052
rs13337052
2 0.925 0.040 16 7323469 intron variant T/C snv 0.23 0.700 1.000 1 2018 2018
dbSNP: rs17138199
rs17138199
2 0.925 0.040 16 5604140 intron variant T/C snv 3.9E-02 0.700 1.000 1 2018 2018
dbSNP: rs8043821
rs8043821
2 0.925 0.040 16 7406864 intron variant T/C snv 0.90 0.700 1.000 1 2018 2018