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: rs1553190285
rs1553190285
1 1.000 1 116384802 missense variant T/G snv 0.800 1.000 1 2018 2018
dbSNP: rs1553192086
rs1553192086
1 1.000 1 116395224 missense variant T/C snv 0.800 1.000 1 2018 2018
dbSNP: rs1553192091
rs1553192091
2 0.925 0.080 1 116395247 missense variant C/A;G snv 0.800 1.000 1 2018 2018
dbSNP: rs1553192783
rs1553192783
1 1.000 1 116399068 missense variant A/C snv 0.800 1.000 1 2018 2018