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: rs1481014
rs1481014
3 0.882 0.160 4 88175999 intron variant C/A;T snv 0.24 0.700 1.000 1 2017 2017
dbSNP: rs1481017
rs1481017
4 0.882 0.160 4 88176325 intron variant C/T snv 0.59 0.700 1.000 1 2017 2017
dbSNP: rs2127863
rs2127863
3 0.882 0.160 4 88190316 intron variant T/C snv 0.84 0.700 1.000 1 2017 2017
dbSNP: rs2622629
rs2622629
4 0.882 0.160 4 88172912 intron variant T/C snv 0.28 0.700 1.000 1 2017 2017
dbSNP: rs7658584
rs7658584
1 1.000 0.040 4 88175489 intron variant G/A snv 0.24 0.700 1.000 1 2017 2017
dbSNP: rs7682521
rs7682521
1 1.000 0.040 4 88175275 intron variant T/G snv 0.24 0.700 1.000 1 2017 2017