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: rs11699306
rs11699306
2 20 35213480 intron variant T/C snv 0.10 0.700 1.000 1 2010 2010
dbSNP: rs12479765
rs12479765
2 20 35237575 intron variant G/A snv 0.17 0.700 1.000 1 2010 2010
dbSNP: rs17092456
rs17092456
2 20 35208389 intron variant G/C snv 0.13 0.700 1.000 1 2010 2010
dbSNP: rs17406518
rs17406518
2 20 35211373 intron variant A/C;G snv 0.700 1.000 1 2010 2010
dbSNP: rs2250205
rs2250205
2 20 35280121 splice region variant G/A snv 0.23 0.25 0.700 1.000 1 2010 2010
dbSNP: rs2275274
rs2275274
2 20 35269741 intron variant C/A;G;T snv 4.2E-04; 0.11 0.700 1.000 1 2010 2010
dbSNP: rs2297789
rs2297789
2 20 35279445 intron variant A/T snv 0.24 0.700 1.000 1 2010 2010
dbSNP: rs2425024
rs2425024
2 20 35257135 intron variant A/C snv 0.34 0.700 1.000 1 2010 2010
dbSNP: rs6060341
rs6060341
2 20 35275830 3 prime UTR variant A/G snv 0.24 0.700 1.000 1 2010 2010
dbSNP: rs6088764
rs6088764
2 20 35205356 intron variant C/A snv 0.38 0.700 1.000 1 2010 2010
dbSNP: rs6088776
rs6088776
2 20 35247970 intron variant T/C snv 0.12 0.700 1.000 1 2010 2010
dbSNP: rs6120870
rs6120870
2 20 35209685 intron variant A/G snv 0.19 0.700 1.000 1 2010 2010