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: rs11679740
rs11679740
1 2 203450671 intron variant G/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs11683935
rs11683935
1 2 203513148 intron variant C/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs11687186
rs11687186
1 2 203455116 intron variant C/G snv 0.43 0.700 1.000 1 2011 2011
dbSNP: rs1376877
rs1376877
1 2 203407367 intron variant C/T snv 0.44 0.700 1.000 1 2011 2011
dbSNP: rs2012774
rs2012774
1 2 203505480 intron variant A/G snv 0.61 0.700 1.000 1 2011 2011
dbSNP: rs2246118
rs2246118
1 2 203462916 intron variant T/C snv 0.62 0.700 1.000 1 2011 2011
dbSNP: rs2246849
rs2246849
1 2 203444602 3 prime UTR variant G/A snv 0.61 0.700 1.000 1 2011 2011
dbSNP: rs2247380
rs2247380
1 2 203499998 intron variant C/T snv 0.60 0.700 1.000 1 2011 2011
dbSNP: rs2250522
rs2250522
1 2 203436573 3 prime UTR variant G/A snv 0.63 0.700 1.000 1 2011 2011
dbSNP: rs2305417
rs2305417
1 2 203495478 intron variant A/G snv 0.42 0.700 1.000 1 2011 2011
dbSNP: rs2352079
rs2352079
1 2 203451809 intron variant C/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs2469953
rs2469953
1 2 203457575 synonymous variant T/C snv 0.58 0.61 0.700 1.000 1 2011 2011
dbSNP: rs2469954
rs2469954
1 2 203427794 3 prime UTR variant T/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs2469962
rs2469962
1 2 203491099 intron variant G/A snv 0.64 0.700 1.000 1 2011 2011
dbSNP: rs3769676
rs3769676
1 2 203401620 intron variant T/C snv 0.26 0.700 1.000 1 2011 2011
dbSNP: rs3769678
rs3769678
1 2 203411604 intron variant T/A;C snv 0.700 1.000 1 2011 2011