Source: ALL
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: rs864309721
rs864309721
CDC42
2 1.000 1 22086451 missense variant A/G snv 0.820 1.000 4 2015 2019
dbSNP: rs1064795845
rs1064795845
CDC42
1 1.000 1 22078540 missense variant T/C snv 0.700 0
dbSNP: rs1553196100
rs1553196100
CDC42
1 1.000 1 22086502 missense variant G/T snv 0.700 0
dbSNP: rs1553196101
rs1553196101
CDC42
8 0.925 0.080 1 22086507 missense variant T/C snv 0.700 0
dbSNP: rs1553196539
rs1553196539
CDC42
1 1.000 1 22091452 missense variant G/A snv 0.700 0
dbSNP: rs797044870
rs797044870
CDC42
3 0.925 1 22086456 missense variant A/G snv 0.700 0