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: rs786205133
rs786205133
RLIM
4 0.882 0.120 X 74592248 missense variant T/C snv 0.800 0
dbSNP: rs1569309449
rs1569309449
RLIM
1 1.000 X 74591484 missense variant G/A snv 0.700 0
dbSNP: rs1569309459
rs1569309459
RLIM
1 1.000 X 74591520 missense variant G/A snv 0.700 0
dbSNP: rs1569309460
rs1569309460
RLIM
1 1.000 X 74591523 missense variant C/T snv 0.700 0
dbSNP: rs1569309474
rs1569309474
RLIM
1 1.000 X 74591555 missense variant G/C snv 0.700 0
dbSNP: rs1569309484
rs1569309484
RLIM
13 0.807 0.200 X 74591586 missense variant A/G snv 0.700 0
dbSNP: rs1569309776
rs1569309776
RLIM
1 1.000 X 74592156 missense variant G/A snv 0.700 0
dbSNP: rs1569309816
rs1569309816
RLIM
1 1.000 X 74592222 missense variant G/A snv 0.700 0