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: rs10167119
rs10167119
3 2 233680666 intron variant T/C snv 0.34 0.700 1.000 1 2013 2013
dbSNP: rs10168155
rs10168155
3 2 233688190 intron variant C/T snv 0.39 0.700 1.000 1 2013 2013
dbSNP: rs10168333
rs10168333
3 2 233688342 intron variant C/T snv 0.39 0.700 1.000 1 2013 2013
dbSNP: rs10168416
rs10168416
1 2 233688441 intron variant C/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs10171367
rs10171367
3 2 233689021 intron variant C/A;G snv 0.700 1.000 1 2013 2013
dbSNP: rs10173355
rs10173355
6 1.000 2 233688675 intron variant A/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs10175809
rs10175809
3 2 233688219 intron variant T/A snv 0.39 0.700 1.000 1 2013 2013
dbSNP: rs10179094
rs10179094
3 2 233689179 intron variant T/A snv 0.34 0.700 1.000 1 2013 2013
dbSNP: rs10197460
rs10197460
3 2 233680544 intron variant G/T snv 0.34 0.700 1.000 1 2013 2013
dbSNP: rs11680450
rs11680450
3 2 233688837 intron variant T/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs11902131
rs11902131
3 2 233685623 intron variant C/T snv 0.39 0.700 1.000 1 2013 2013
dbSNP: rs13002774
rs13002774
3 2 233685060 intron variant G/A;T snv 0.700 1.000 1 2013 2013
dbSNP: rs4261716
rs4261716
3 2 233684471 intron variant G/T snv 0.39 0.700 1.000 1 2013 2013
dbSNP: rs4347832
rs4347832
3 2 233684395 intron variant T/C snv 0.39 0.700 1.000 1 2013 2013
dbSNP: rs4530361
rs4530361
3 2 233681395 intron variant A/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs4553819
rs4553819
3 2 233685437 intron variant A/G snv 0.39 0.700 1.000 1 2013 2013
dbSNP: rs6724485
rs6724485
3 2 233684170 intron variant G/A snv 0.39 0.700 1.000 1 2013 2013
dbSNP: rs6736508
rs6736508
3 2 233687101 intron variant G/A snv 0.39 0.700 1.000 1 2013 2013
dbSNP: rs6736743
rs6736743
3 2 233687304 intron variant G/A snv 0.39 0.700 1.000 1 2013 2013
dbSNP: rs6753320
rs6753320
3 2 233686969 intron variant A/C snv 0.39 0.700 1.000 1 2013 2013
dbSNP: rs6753569
rs6753569
3 2 233687171 intron variant A/C snv 0.39 0.700 1.000 1 2013 2013
dbSNP: rs7577677
rs7577677
3 2 233681970 synonymous variant C/A;G;T snv 0.35; 1.6E-05; 4.0E-06 0.700 1.000 1 2013 2013
dbSNP: rs7586110
rs7586110
3 2 233681881 intron variant T/A;G snv 0.700 1.000 1 2013 2013
dbSNP: rs10445704
rs10445704
3 2 233691628 5 prime UTR variant G/A snv 0.39 0.700 1.000 1 2013 2013
dbSNP: rs12623271
rs12623271
3 2 233691295 3 prime UTR variant C/G snv 0.39 0.700 1.000 1 2013 2013