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: rs1156413585
rs1156413585
1 1.000 0.160 9 35657978 non coding transcript exon variant C/T snv 7.7E-06 0.700 1.000 3 2005 2010
dbSNP: rs1218494857
rs1218494857
1 1.000 0.160 9 35658018 upstream gene variant -/TCTCAGCTTCACAGAGACGT;TCTCAGCTTCACAGAGTACGT;TCTCAGCTTTACGT delins 0.700 0
dbSNP: rs121909638
rs121909638
3 0.882 0.280 8 38421853 missense variant A/G snv 0.010 1.000 1 2017 2017
dbSNP: rs121912521
rs121912521
2 0.925 0.200 2 48688067 missense variant G/A snv 0.010 1.000 1 2008 2008
dbSNP: rs1230629953
rs1230629953
1 1.000 0.160 9 35658025 upstream gene variant -/CTTCACAG;CTTCACAGCTTCACAG;TCCCCAGCTTCACAG delins 1.4E-05 0.700 0
dbSNP: rs1554651153
rs1554651153
1 1.000 0.160 9 35657836 non coding transcript exon variant C/A;G;T snv 0.700 1.000 5 2005 2015
dbSNP: rs1554651364
rs1554651364
1 1.000 0.160 9 35658016 non coding transcript exon variant -/TCTCAGCTTCCACGT delins 0.700 1.000 4 2001 2007
dbSNP: rs1554651365
rs1554651365
1 1.000 0.160 9 35658016 non coding transcript exon variant -/CACGTCCTC delins 0.700 0
dbSNP: rs1554651368
rs1554651368
1 1.000 0.160 9 35658017 non coding transcript exon variant -/TCTCAGCTCACGT;TCTCAGCTTCACAGACACGT;TCTCAGCTTCACAGAGCACGT delins 0.700 0
dbSNP: rs1554651373
rs1554651373
1 1.000 0.160 9 35658017 non coding transcript exon variant -/GTCCTCAGCTTCAC delins 0.700 1.000 1 2002 2002
dbSNP: rs1554651382
rs1554651382
1 1.000 0.160 9 35658017 non coding transcript exon variant -/CACGTCCTCAGCTTCACAGA delins 0.700 1.000 4 2001 2007
dbSNP: rs1554651393
rs1554651393
1 1.000 0.160 9 35658018 upstream gene variant -/ACGTCCTCAG delins 0.700 1.000 3 2001 2007
dbSNP: rs1554651395
rs1554651395
1 1.000 0.160 9 35658018 upstream gene variant -/AACGTCCTCAGCTTCA delins 0.700 1.000 3 2001 2007
dbSNP: rs1554651396
rs1554651396
1 1.000 0.160 9 35658018 upstream gene variant -/CGTCCTCAGCTTCACAGA delins 0.700 1.000 4 2001 2007
dbSNP: rs1554651397
rs1554651397
1 1.000 0.160 9 35658018 upstream gene variant -/TACGTCCTCAGCTTCACAGAGT delins 0.700 0
dbSNP: rs1554651400
rs1554651400
1 1.000 0.160 9 35658019 upstream gene variant -/CGTCCTCAGCTTC;GTCCTCAGCTTC delins 0.700 1.000 1 2002 2002
dbSNP: rs1554651403
rs1554651403
1 1.000 0.160 9 35658019 upstream gene variant -/CGTCCTCAGCTTCACAGAGT delins 0.700 0
dbSNP: rs1554651404
rs1554651404
2 0.925 0.200 9 35658019 upstream gene variant -/CGTCCTCAGCTTCACAGAG delins 0.700 0
dbSNP: rs1554651405
rs1554651405
1 1.000 0.160 9 35658020 upstream gene variant -/TCTCAGCTTCACAGAGT;TCTCAGCTTCACAGAGTAGT;TCTCAGCTTCACAGAGTGGT delins 0.700 0
dbSNP: rs1554651411
rs1554651411
1 1.000 0.160 9 35658020 upstream gene variant -/CCTCAGCTTCACAGAGTAGT;GTCCTCAGCTTCACAGAGTAGT delins 0.700 1.000 6 2001 2007
dbSNP: rs1554651413
rs1554651413
2 0.925 0.200 9 35658020 upstream gene variant -/GTCCTCAGCTTCACAGAGTAGTA delins 0.700 1.000 4 2001 2007
dbSNP: rs1554651418
rs1554651418
1 1.000 0.160 9 35658020 upstream gene variant -/GTCCTCAGCTTCACAGAG delins 0.700 0
dbSNP: rs1554651422
rs1554651422
1 1.000 0.160 9 35658021 upstream gene variant -/TCCTCAGCTTCAC delins 0.700 1.000 4 2001 2007
dbSNP: rs1554651424
rs1554651424
1 1.000 0.160 9 35658021 upstream gene variant -/TCCTCAGCTT delins 0.700 0
dbSNP: rs1554651425
rs1554651425
1 1.000 0.160 9 35658021 upstream gene variant -/CTCAGCTTC delins 0.700 0