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: rs10649609
rs10649609
1 2 164696196 non coding transcript exon variant -/AATAA;AGTAA delins 0.700 1.000 1 2016 2016
dbSNP: rs1128249
rs1128249
10 1.000 0.080 2 164672114 intron variant G/C;T snv 0.700 1.000 1 2016 2016
dbSNP: rs13389219
rs13389219
9 1.000 0.080 2 164672366 intron variant C/T snv 0.47 0.700 1.000 1 2016 2016
dbSNP: rs6712203
rs6712203
2 2 164700808 intron variant C/T snv 0.34 0.45 0.700 1.000 1 2016 2016