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: rs11662308
rs11662308
1 18 21585516 intron variant T/G snv 0.15 0.700 1.000 1 2018 2018
dbSNP: rs12373434
rs12373434
1 18 21532778 intron variant T/C;G snv 0.700 1.000 1 2018 2018
dbSNP: rs973730
rs973730
1 18 21573533 synonymous variant C/T snv 0.84 0.83 0.700 1.000 1 2018 2018