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: rs1167998
rs1167998
5 1 62465961 intron variant C/A snv 0.57 0.800 1.000 2 2009 2019
dbSNP: rs1748195
rs1748195
3 0.851 0.120 1 62583922 intron variant C/G;T snv 0.800 1.000 2 2008 2019
dbSNP: rs2131925
rs2131925
5 1 62560271 intron variant G/T snv 0.57 0.800 1.000 2 2010 2019
dbSNP: rs10889353
rs10889353
3 1 62652525 intron variant A/C;T snv 0.800 1.000 1 2009 2019
dbSNP: rs1168013
rs1168013
2 1.000 0.120 1 62531167 intron variant C/G;T snv 0.800 1.000 1 2010 2019
dbSNP: rs1748197
rs1748197
5 1 62590441 intron variant G/A snv 0.42 0.700 1.000 2 2012 2012
dbSNP: rs10789117
rs10789117
5 1 62606594 intron variant A/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs11207997
rs11207997
5 1 62596235 intron variant C/T snv 0.39 0.700 1.000 1 2012 2012
dbSNP: rs12048208
rs12048208
2 1 62589609 intron variant G/A snv 0.12 0.700 1.000 1 2012 2012