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: rs10162249
rs10162249
1 1.000 0.040 13 25849519 intron variant T/C snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs10467674
rs10467674
1 1.000 0.040 13 25854100 intron variant T/A snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs112198380
rs112198380
1 1.000 0.040 13 25855238 intron variant A/G snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs12020004
rs12020004
1 1.000 0.040 13 25851513 intron variant G/A snv 0.13 0.700 1.000 1 2012 2012
dbSNP: rs61949368
rs61949368
1 1.000 0.040 13 25854979 intron variant G/A snv 0.13 0.700 1.000 1 2012 2012
dbSNP: rs9319247
rs9319247
1 1.000 0.040 13 25848959 intron variant T/C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs9319248
rs9319248
1 1.000 0.040 13 25849030 intron variant C/A snv 0.13 0.700 1.000 1 2012 2012
dbSNP: rs9319249
rs9319249
1 1.000 0.040 13 25854051 intron variant T/C snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs9319250
rs9319250
1 1.000 0.040 13 25854469 intron variant T/C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs9507586
rs9507586
1 1.000 0.040 13 25852156 intron variant A/T snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs9507587
rs9507587
1 1.000 0.040 13 25852362 intron variant G/A snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs9507588
rs9507588
1 1.000 0.040 13 25852698 intron variant C/T snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs9507589
rs9507589
1 1.000 0.040 13 25852835 intron variant T/C snv 0.13 0.700 1.000 1 2012 2012
dbSNP: rs9511937
rs9511937
1 1.000 0.040 13 25849760 intron variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs9511938
rs9511938
1 1.000 0.040 13 25849774 intron variant A/G snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs9511939
rs9511939
1 1.000 0.040 13 25850518 intron variant T/G snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs9511941
rs9511941
1 1.000 0.040 13 25850692 intron variant A/G snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs9511942
rs9511942
1 1.000 0.040 13 25850702 intron variant G/A snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs9511943
rs9511943
1 1.000 0.040 13 25850921 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs9511944
rs9511944
1 1.000 0.040 13 25850925 intron variant T/A snv 0.13 0.700 1.000 1 2012 2012
dbSNP: rs9511945
rs9511945
1 1.000 0.040 13 25851056 intron variant C/G snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs9511946
rs9511946
1 1.000 0.040 13 25851130 intron variant A/G snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs9511947
rs9511947
1 1.000 0.040 13 25851239 intron variant G/A snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs9511949
rs9511949
1 1.000 0.040 13 25851476 intron variant G/A snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs9511950
rs9511950
1 1.000 0.040 13 25851514 intron variant C/A snv 0.13 0.700 1.000 1 2012 2012