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: rs11676272
rs11676272
5 1.000 0.040 2 24918669 missense variant A/G snv 0.47 0.57 0.700 1.000 4 2015 2019
dbSNP: rs10203386
rs10203386
1 2 24913997 intron variant T/A;G snv 0.700 1.000 2 2019 2019
dbSNP: rs6545814
rs6545814
3 2 24908447 intron variant A/G snv 0.53 0.700 1.000 2 2012 2014
dbSNP: rs10203482
rs10203482
1 2 24914047 intron variant T/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs1529897
rs1529897
1 2 24863958 intron variant T/A;G snv 0.700 1.000 1 2019 2019
dbSNP: rs4077678
rs4077678
1 2 24899971 intron variant C/G snv 0.55 0.700 1.000 1 2017 2017
dbSNP: rs6737082
rs6737082
1 2 24915171 intron variant A/C snv 0.56 0.700 1.000 1 2015 2015
dbSNP: rs7586879
rs7586879
3 2 24894108 intron variant C/T snv 0.47 0.700 1.000 1 2013 2013