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: rs13078960
rs13078960
2 3 85758440 intron variant T/G snv 0.15 0.700 1.000 1 2017 2017
dbSNP: rs34495106
rs34495106
1 3 85601986 intron variant A/G snv 0.51 0.700 1.000 1 2019 2019
dbSNP: rs3911063
rs3911063
2 1.000 0.040 3 85857778 intron variant T/C snv 0.30 0.700 1.000 1 2019 2019