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: rs139961185
rs139961185
2 11 116936627 intron variant G/A snv 1.1E-02 0.800 1.000 3 2014 2019
dbSNP: rs2075292
rs2075292
1 11 116861796 intron variant G/T snv 0.80 0.86 0.800 1.000 3 2008 2019
dbSNP: rs12225230
rs12225230
4 11 116857914 missense variant G/A;C;T snv 1.2E-05; 0.19; 4.0E-06 0.800 1.000 2 2012 2018
dbSNP: rs7115242
rs7115242
16 0.851 0.120 11 117037567 intron variant A/G;T snv 0.700 1.000 2 2016 2018
dbSNP: rs10047459
rs10047459
1 11 116851110 intron variant C/T snv 0.80 0.700 1.000 1 2012 2012
dbSNP: rs10047462
rs10047462
3 11 116851325 intron variant G/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs11216162
rs11216162
3 11 116857561 non coding transcript exon variant G/A snv 0.17 0.700 1.000 1 2012 2012
dbSNP: rs12099358
rs12099358
2 11 116855332 non coding transcript exon variant C/A snv 0.24 0.700 1.000 1 2012 2012
dbSNP: rs1351452
rs1351452
1 11 117072638 intron variant A/C snv 0.86 0.700 1.000 1 2009 2009
dbSNP: rs17120139
rs17120139
1 11 116903485 intron variant G/A snv 0.13 0.700 1.000 1 2008 2008
dbSNP: rs4938315
rs4938315
2 11 116860489 intron variant G/A snv 0.85 0.700 1.000 1 2012 2012
dbSNP: rs548638
rs548638
1 11 116866377 intron variant T/G snv 0.15 0.700 1.000 1 2012 2012
dbSNP: rs588918
rs588918
1 11 116985926 intron variant T/C snv 0.86 0.700 1.000 1 2009 2009
dbSNP: rs625145
rs625145
1 11 116857220 non coding transcript exon variant A/T snv 0.32 0.700 1.000 1 2012 2012
dbSNP: rs689243
rs689243
2 11 116851977 intron variant G/C snv 0.46 0.700 1.000 1 2012 2012
dbSNP: rs7124741
rs7124741
1 11 116881503 intron variant A/G;T snv 0.700 1.000 1 2008 2008
dbSNP: rs888245
rs888245
1 11 116853021 intron variant C/G snv 0.16 0.700 1.000 1 2012 2012
dbSNP: rs888246
rs888246
1 11 116853516 intron variant C/T snv 8.6E-02 0.700 1.000 1 2012 2012