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: rs174589
rs174589
1 11 61848331 intron variant C/G;T snv 0.19 0.700 1.000 1 2011 2011
dbSNP: rs695867
rs695867
1 11 61793816 intron variant A/G snv 2.6E-02 0.700 1.000 1 2011 2011
dbSNP: rs17156426
rs17156426
2 11 61841851 intron variant A/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs17156442
rs17156442
2 11 61846551 intron variant C/T snv 0.11 0.700 1.000 1 2011 2011
dbSNP: rs174579
rs174579
2 11 61838141 intron variant C/T snv 0.16 0.700 1.000 1 2011 2011
dbSNP: rs174585
rs174585
2 11 61844222 intron variant G/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs174591
rs174591
2 11 61850204 intron variant T/A;G snv 0.700 1.000 1 2011 2011
dbSNP: rs174593
rs174593
2 11 61851359 intron variant T/C snv 0.24 0.700 1.000 1 2011 2011
dbSNP: rs174597
rs174597
2 11 61853568 intron variant G/A;C;T snv 0.700 1.000 1 2011 2011
dbSNP: rs174605
rs174605
2 11 61859449 intron variant G/T snv 0.20 0.700 1.000 1 2011 2011
dbSNP: rs174611
rs174611
2 11 61860409 intron variant T/C snv 0.21 0.700 1.000 1 2011 2011
dbSNP: rs17764324
rs17764324
2 11 61867616 downstream gene variant G/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs17831757
rs17831757
2 11 61867728 downstream gene variant T/C snv 9.3E-02 0.700 1.000 1 2011 2011
dbSNP: rs2524299
rs2524299
2 11 61837310 intron variant A/T snv 0.17 0.700 1.000 1 2011 2011
dbSNP: rs2526678
rs2526678
2 11 61856321 non coding transcript exon variant G/A snv 8.6E-02 0.700 1.000 1 2011 2011
dbSNP: rs2727270
rs2727270
2 11 61835765 intron variant C/T snv 0.12 0.700 1.000 1 2011 2011
dbSNP: rs2727271
rs2727271
2 11 61835886 intron variant A/T snv 0.12 0.700 1.000 1 2011 2011
dbSNP: rs7935946
rs7935946
2 11 61848070 5 prime UTR variant C/T snv 0.11 0.700 1.000 1 2011 2011
dbSNP: rs916924
rs916924
2 11 61851709 intron variant T/C snv 9.1E-02 0.700 1.000 1 2011 2011
dbSNP: rs174575
rs174575
3 1.000 0.040 11 61834531 intron variant C/G snv 0.25 0.700 1.000 1 2011 2011
dbSNP: rs174602
rs174602
3 1.000 0.080 11 61856942 non coding transcript exon variant T/C snv 0.37 0.700 1.000 1 2011 2011
dbSNP: rs174616
rs174616
3 1.000 0.080 11 61861650 intron variant G/A snv 0.51 0.700 1.000 1 2011 2011
dbSNP: rs2845573
rs2845573
3 1.000 0.040 11 61834436 intron variant A/G snv 9.7E-02 0.700 1.000 1 2011 2011
dbSNP: rs498793
rs498793
3 1.000 0.040 11 61857233 intron variant T/C snv 0.62 0.700 1.000 1 2011 2011
dbSNP: rs526126
rs526126
3 1.000 0.040 11 61857413 intron variant G/C;T snv 0.81; 8.0E-06 0.700 1.000 1 2011 2011