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: rs121918150
rs121918150
PROC ; LOC105373608
2 0.925 0.080 2 127428560 missense variant G/A;T snv 8.0E-06 0.800 1.000 7 1992 2015
dbSNP: rs121918151
rs121918151
PROC ; LOC105373608
1 1.000 0.080 2 127428426 missense variant C/T snv 0.800 1.000 7 1992 2015
dbSNP: rs121918143
rs121918143
PROC ; LOC105373608
3 0.882 0.080 2 127426180 missense variant C/A;T snv 4.0E-06; 2.8E-05 0.700 0
dbSNP: rs121918144
rs121918144
PROC ; LOC105373608
1 1.000 0.080 2 127428462 missense variant C/T snv 0.700 0
dbSNP: rs121918146
rs121918146
PROC ; LOC105373608
5 0.827 0.200 2 127428485 missense variant G/A snv 1.2E-05 2.1E-05 0.700 0
dbSNP: rs121918147
rs121918147
PROC ; LOC105373608
1 1.000 0.080 2 127428587 missense variant G/A snv 4.0E-06 0.700 0
dbSNP: rs121918148
rs121918148
PROC
2 0.925 0.080 2 127421397 missense variant A/C snv 0.700 0
dbSNP: rs121918149
rs121918149
PROC
3 0.882 0.080 2 127421438 missense variant G/A snv 5.2E-05 7.7E-05 0.700 0
dbSNP: rs121918156
rs121918156
PROC ; LOC105373608
3 0.882 0.120 2 127427219 missense variant C/T snv 0.700 0
dbSNP: rs121918157
rs121918157
PROC ; LOC105373608
1 1.000 0.080 2 127428895 missense variant C/G snv 4.0E-06 7.0E-06 0.700 0
dbSNP: rs1254257945
rs1254257945
PROC ; MIR4783
1 1.000 0.080 2 127423405 missense variant G/A;C snv 6.8E-06; 4.1E-05 0.700 0
dbSNP: rs767730328
rs767730328
PROC ; LOC105373608
2 0.925 0.080 2 127428660 missense variant T/C snv 4.0E-06 0.700 0