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: rs8027411
rs8027411
4 0.882 0.040 15 79168687 intron variant G/T snv 0.52 0.710 1.000 1 2010 2010
dbSNP: rs11072826
rs11072826
1 15 79169174 intron variant A/G snv 0.40 0.700 1.000 1 2010 2010
dbSNP: rs11629665
rs11629665
1 15 79164791 intron variant G/A;C snv 0.52 0.700 1.000 1 2010 2010
dbSNP: rs11631411
rs11631411
1 15 79153474 intron variant C/T snv 0.40 0.700 1.000 1 2010 2010
dbSNP: rs11634903
rs11634903
1 15 79143850 intron variant A/C;G snv 0.700 1.000 1 2010 2010
dbSNP: rs11638625
rs11638625
1 15 79142445 non coding transcript exon variant T/G snv 0.37 0.700 1.000 1 2010 2010
dbSNP: rs12439908
rs12439908
1 15 79164039 intron variant T/C snv 0.51 0.700 1.000 1 2010 2010
dbSNP: rs17175798
rs17175798
3 0.925 0.040 15 79171618 intron variant C/A;T snv 0.700 1.000 1 2010 2010
dbSNP: rs2204069
rs2204069
1 15 79156993 intron variant A/G snv 0.48 0.700 1.000 1 2010 2010
dbSNP: rs4778651
rs4778651
1 15 79155468 intron variant G/A;C snv 0.700 1.000 1 2010 2010
dbSNP: rs4778924
rs4778924
1 15 79151021 intron variant T/C snv 0.43 0.700 1.000 1 2010 2010
dbSNP: rs8031019
rs8031019
1 15 79166170 intron variant A/G snv 0.54 0.700 1.000 1 2010 2010
dbSNP: rs8031504
rs8031504
1 15 79166247 intron variant G/C;T snv 0.700 1.000 1 2010 2010
dbSNP: rs8033963
rs8033963
1 15 79163008 intron variant C/T snv 0.51 0.700 1.000 1 2010 2010
dbSNP: rs939658
rs939658
2 1.000 15 79159527 intron variant A/G snv 0.53 0.700 1.000 1 2010 2010