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: rs2494250
rs2494250
1 1 159308461 downstream gene variant G/C;T snv 0.700 1.000 2 2007 2012
dbSNP: rs16841987
rs16841987
1 1 159295476 intron variant G/A snv 0.16 0.700 1.000 1 2012 2012
dbSNP: rs2427824
rs2427824
2 1.000 0.040 1 159295272 intron variant T/C snv 0.79 0.700 1.000 1 2012 2012
dbSNP: rs2427825
rs2427825
1 1 159296276 intron variant T/C snv 0.79 0.700 1.000 1 2012 2012
dbSNP: rs2427828
rs2427828
1 1 159303251 intron variant G/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs2494263
rs2494263
1 1 159286004 upstream gene variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs2494265
rs2494265
1 1 159305484 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs3845625
rs3845625
1 1 159296086 intron variant C/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs7549785
rs7549785
3 0.925 0.080 1 159308078 3 prime UTR variant G/A snv 0.13 0.700 1.000 1 2012 2012