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: rs6830062
rs6830062
2 4 18016107 intron variant T/C snv 0.25 0.700 1.000 2 2008 2009
dbSNP: rs925098
rs925098
3 4 17918188 intron variant G/A snv 0.70 0.700 1.000 2 2011 2012
dbSNP: rs1380294
rs1380294
2 4 18022498 upstream gene variant C/T snv 0.25 0.700 1.000 1 2011 2011
dbSNP: rs16896068
rs16896068
2 4 17943217 intron variant G/A snv 0.25 0.700 1.000 1 2008 2008
dbSNP: rs16896210
rs16896210
1 4 17990709 intron variant A/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs16896261
rs16896261
1 4 18009579 intron variant A/G snv 0.21 0.700 1.000 1 2011 2011
dbSNP: rs2011603
rs2011603
1 4 18023861 upstream gene variant G/A snv 0.70 0.700 1.000 1 2012 2012
dbSNP: rs2320299
rs2320299
1 4 17970749 intron variant G/A snv 0.69 0.700 1.000 1 2011 2011
dbSNP: rs2707450
rs2707450
3 4 17940937 intron variant C/T snv 0.73 0.700 1.000 1 2011 2011
dbSNP: rs2724475
rs2724475
2 4 17944809 intron variant T/C snv 0.71 0.700 1.000 1 2010 2010
dbSNP: rs6844379
rs6844379
1 4 17855178 intron variant C/T snv 0.70 0.700 1.000 1 2011 2011
dbSNP: rs6845078
rs6845078
2 4 17950585 intron variant C/A;T snv 0.700 1.000 1 2013 2013
dbSNP: rs6853216
rs6853216
1 4 17969032 intron variant C/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs724577
rs724577
3 4 17991787 intron variant A/C snv 0.71 0.700 1.000 1 2011 2011
dbSNP: rs7663818
rs7663818
1 4 17934820 intron variant C/T snv 0.23 0.700 1.000 1 2011 2011
dbSNP: rs7692995
rs7692995
2 4 17935011 intron variant T/C snv 0.23 0.700 1.000 1 2011 2011