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: rs2524163
rs2524163
4 0.925 0.160 6 31291802 intron variant C/T snv 0.66 0.700 1.000 1 2012 2012
dbSNP: rs2596475
rs2596475
1 1.000 0.040 6 31358547 upstream gene variant C/G;T snv 0.68 0.700 1.000 1 2012 2012
dbSNP: rs2844595
rs2844595
1 1.000 0.040 6 31290478 intron variant G/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs2844603
rs2844603
1 1.000 0.040 6 31283077 intron variant A/G snv 0.66 0.700 1.000 1 2012 2012
dbSNP: rs2844608
rs2844608
1 1.000 0.040 6 31279637 intron variant C/T snv 0.39 0.700 1.000 1 2012 2012
dbSNP: rs2853918
rs2853918
2 0.925 0.160 6 31300843 intron variant C/T snv 0.65 0.700 1.000 1 2012 2012
dbSNP: rs2853921
rs2853921
1 1.000 0.040 6 31299284 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs2853922
rs2853922
1 1.000 0.040 6 31298413 intron variant A/G snv 0.65 0.700 1.000 1 2012 2012
dbSNP: rs2853931
rs2853931
1 1.000 0.040 6 31287230 intron variant C/A;G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs2853933
rs2853933
2 0.925 0.160 6 31286311 intron variant T/C snv 0.66 0.700 1.000 1 2012 2012
dbSNP: rs2853935
rs2853935
1 1.000 0.040 6 31286101 intron variant C/T snv 0.66 0.700 1.000 1 2012 2012
dbSNP: rs2853938
rs2853938
1 1.000 0.040 6 31283700 intron variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs2853939
rs2853939
2 0.925 0.160 6 31282865 intron variant T/C snv 0.66 0.700 1.000 1 2012 2012
dbSNP: rs6457375
rs6457375
1 1.000 0.040 6 31304835 intron variant G/A snv 0.55 0.700 1.000 1 2012 2012
dbSNP: rs6931332
rs6931332
1 1.000 0.040 6 31306468 intron variant A/C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs7766089
rs7766089
1 1.000 0.040 6 31281816 intron variant G/A snv 0.68 0.700 1.000 1 2012 2012
dbSNP: rs9264873
rs9264873
1 1.000 0.040 6 31303923 intron variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs9265645
rs9265645
1 1.000 0.040 6 31332420 intron variant G/A snv 8.7E-02 0.700 1.000 1 2012 2012
dbSNP: rs9265961
rs9265961
1 1.000 0.040 6 31347724 intron variant A/C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs9265969
rs9265969
1 1.000 0.040 6 31347929 intron variant G/A snv 0.12 0.700 1.000 1 2012 2012
dbSNP: rs9266214
rs9266214
1 1.000 0.040 6 31357272 non coding transcript exon variant G/A;C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs9266230
rs9266230
1 1.000 0.040 6 31357564 non coding transcript exon variant G/C snv 0.72 0.700 1.000 1 2012 2012
dbSNP: rs9266231
rs9266231
1 1.000 0.040 6 31357603 non coding transcript exon variant C/T snv 0.72 0.700 1.000 1 2012 2012
dbSNP: rs9266232
rs9266232
1 1.000 0.040 6 31357647 upstream gene variant G/T snv 0.72 0.700 1.000 1 2012 2012
dbSNP: rs9266242
rs9266242
1 1.000 0.040 6 31357843 upstream gene variant T/C snv 0.72 0.700 1.000 1 2012 2012