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: rs10762524
rs10762524
1 1.000 0.040 10 52014152 intron variant T/A;C;G snv 0.700 1.000 1 2010 2010
dbSNP: rs10823964
rs10823964
1 1.000 0.040 10 52017283 intron variant T/G snv 0.51 0.700 1.000 1 2010 2010
dbSNP: rs10823973
rs10823973
1 1.000 0.040 10 52019720 intron variant C/G;T snv 0.700 1.000 1 2010 2010