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: rs10168416
rs10168416
1 2 233688441 intron variant C/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs10202865
rs10202865
1 2 233679061 intron variant C/T snv 0.30 0.700 1.000 1 2013 2013
dbSNP: rs13009407
rs13009407
1 2 233743701 non coding transcript exon variant C/A;G;T snv 4.0E-06; 0.22; 4.0E-06 0.700 1.000 1 2013 2013
dbSNP: rs2602374
rs2602374
1 2 233660318 intron variant C/T snv 0.21 0.700 1.000 1 2013 2013
dbSNP: rs2741044
rs2741044
1 2 233670722 intron variant G/A snv 0.22 0.700 1.000 1 2013 2013
dbSNP: rs28899170
rs28899170
1 2 233695584 intron variant C/A;T snv 0.700 1.000 1 2013 2013
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: rs10171367
rs10171367
3 2 233689021 intron variant C/A;G 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: rs10445704
rs10445704
3 2 233691628 5 prime UTR variant G/A snv 0.39 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: rs12623271
rs12623271
3 2 233691295 3 prime UTR variant C/G 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: rs13015720
rs13015720
3 2 233692353 intron variant G/A snv 0.39 0.700 1.000 1 2013 2013
dbSNP: rs1604144
rs1604144
3 2 233697189 intron variant C/T snv 0.33 0.700 1.000 1 2013 2013
dbSNP: rs17862866
rs17862866
3 2 233702266 intron variant A/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs17864683
rs17864683
3 2 233670563 intron variant A/C;G snv 0.700 1.000 1 2013 2013
dbSNP: rs17864701
rs17864701
3 2 233744071 intron variant C/T snv 0.30 0.700 1.000 1 2013 2013
dbSNP: rs1983023
rs1983023
3 2 233728376 intron variant T/C snv 0.46 0.700 1.000 1 2013 2013
dbSNP: rs2008595
rs2008595
3 2 233728546 intron variant C/T snv 0.56 0.700 1.000 1 2013 2013