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: rs12593813
rs12593813
2 1.000 0.080 15 67744514 intron variant A/G snv 0.53 0.810 1.000 3 2007 2018
dbSNP: rs1026732
rs1026732
1 1.000 0.080 15 67802747 intron variant G/A snv 0.38 0.720 1.000 3 2007 2018
dbSNP: rs11635424
rs11635424
1 1.000 0.080 15 67745240 intron variant A/G snv 0.53 0.710 1.000 2 2007 2018
dbSNP: rs3784709
rs3784709
1 1.000 0.080 15 67779937 intron variant C/T snv 0.36 0.710 1.000 2 2007 2018
dbSNP: rs4489954
rs4489954
1 1.000 0.080 15 67779737 intron variant T/A;G snv 0.710 1.000 2 2007 2018
dbSNP: rs868036
rs868036
1 1.000 0.080 15 67762675 intron variant T/A snv 0.62 0.700 1.000 1 2017 2017
dbSNP: rs41305272
rs41305272
6 0.851 0.120 15 67807105 3 prime UTR variant C/T snv 2.4E-02 0.010 1.000 1 2014 2014