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: rs4663967
rs4663967
3 2 233744538 intron variant A/C snv 0.55 0.700 1.000 1 2013 2013
dbSNP: rs7597496
rs7597496
3 2 233721797 non coding transcript exon variant A/C;G snv 0.700 1.000 1 2013 2013
dbSNP: rs3755319
rs3755319
8 0.925 0.120 2 233758936 intron variant A/C;G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs2018985
rs2018985
3 2 233740214 intron variant A/G snv 0.47 0.700 1.000 1 2013 2013
dbSNP: rs3806597
rs3806597
3 2 233728923 intron variant A/G snv 0.56 0.700 1.000 1 2013 2013
dbSNP: rs4294999
rs4294999
3 2 233726821 intron variant A/G snv 0.54 0.700 1.000 1 2013 2013
dbSNP: rs6431628
rs6431628
3 2 233738832 intron variant A/G snv 0.56 0.700 1.000 1 2013 2013
dbSNP: rs6741669
rs6741669
3 2 233744546 intron variant A/G snv 0.55 0.700 1.000 1 2013 2013
dbSNP: rs7574296
rs7574296
3 2 233729603 synonymous variant A/G snv 0.49 0.54 0.700 1.000 1 2013 2013
dbSNP: rs929596
rs929596
9 0.925 0.040 2 233765830 intron variant A/G snv 0.32 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: rs10929301
rs10929301
4 2 233755003 splice region variant C/G;T snv 0.48 0.700 1.000 1 2013 2013
dbSNP: rs1875263
rs1875263
7 1.000 2 233716976 intron variant C/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs4663971
rs4663971
3 2 233765606 intron variant C/G;T snv 0.50 0.700 1.000 1 2013 2013
dbSNP: rs887829
rs887829
18 0.763 0.280 2 233759924 intron variant C/T snv 0.36 0.700 1.000 2 2013 2014
dbSNP: rs17864701
rs17864701
3 2 233744071 intron variant C/T snv 0.30 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
dbSNP: rs4148325
rs4148325
11 0.851 0.080 2 233764663 intron variant C/T snv 0.36 0.700 1.000 1 2013 2013
dbSNP: rs7604115
rs7604115
4 2 233749470 intron variant C/T snv 0.37 0.700 1.000 1 2013 2013
dbSNP: rs10929302
rs10929302
4 2 233757136 intron variant G/A snv 0.30 0.700 1.000 1 2013 2013
dbSNP: rs11891311
rs11891311
4 2 233730664 intron variant G/A snv 0.42 0.700 1.000 1 2013 2013
dbSNP: rs17862875
rs17862875
4 2 233740656 intron variant G/A snv 0.30 0.700 1.000 1 2013 2013
dbSNP: rs6747843
rs6747843
3 2 233755708 non coding transcript exon variant G/A snv 0.30 0.700 1.000 1 2013 2013
dbSNP: rs869283
rs869283
3 2 233717641 intron variant G/A snv 0.48 0.700 1.000 1 2013 2013
dbSNP: rs11673726
rs11673726
4 2 233755414 non coding transcript exon variant G/A;T snv 0.700 1.000 1 2013 2013