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: rs11675251
rs11675251
1 2 203384676 intron variant A/G snv 0.44 0.800 1.000 1 2011 2011
dbSNP: rs11686036
rs11686036
1 2 203376916 intron variant A/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs12466364
rs12466364
1 2 203361608 intron variant A/G snv 0.22 0.700 1.000 1 2011 2011
dbSNP: rs12474416
rs12474416
1 2 203361280 intron variant G/T snv 0.22 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: rs2246849
rs2246849
1 2 203444602 3 prime UTR variant G/A snv 0.61 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: rs2469954
rs2469954
1 2 203427794 3 prime UTR variant T/A;C snv 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