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: rs12437854
rs12437854
2 0.925 0.080 15 93598604 intron variant T/G snv 0.10 0.030 1.000 3 2012 2014
dbSNP: rs12460876
rs12460876
4 1.000 0.080 19 32865985 intron variant T/C snv 0.36 0.700 1.000 2 2010 2018
dbSNP: rs6420094
rs6420094
5 1.000 0.080 5 177390635 intron variant A/G snv 0.29 0.700 1.000 2 2010 2016
dbSNP: rs7422339
rs7422339
5 1.000 0.080 2 210675783 missense variant C/A snv 0.700 1.000 2 2010 2016
dbSNP: rs7583877
rs7583877
2 0.925 0.080 2 99844192 intron variant C/T snv 0.61 0.020 1.000 2 2012 2013
dbSNP: rs7805747
rs7805747
5 1.000 0.080 7 151710715 intron variant G/A snv 0.26 0.700 1.000 2 2010 2016
dbSNP: rs10109414
rs10109414
5 1.000 0.080 8 23893638 regulatory region variant C/T snv 0.37 0.700 1.000 1 2010 2010
dbSNP: rs10137082
rs10137082
2 0.925 0.080 14 23370824 upstream gene variant C/T snv 0.23 0.010 1.000 1 2012 2012
dbSNP: rs10178409
rs10178409
2 1.000 0.080 2 73628380 downstream gene variant G/T snv 0.26 0.700 1.000 1 2018 2018
dbSNP: rs1020120
rs1020120
2 1.000 0.080 9 84611173 intron variant C/T snv 0.60 0.700 1.000 1 2018 2018
dbSNP: rs102274
rs102274
3 1.000 0.080 11 61790354 non coding transcript exon variant T/C snv 0.28 0.700 1.000 1 2018 2018
dbSNP: rs10404257
rs10404257
2 0.925 0.080 19 38645846 upstream gene variant G/A snv 0.50 0.010 1.000 1 2012 2012
dbSNP: rs1044261
rs1044261
3 1.000 0.080 10 1019770 stop gained C/T snv 5.0E-02 6.0E-02 0.700 1.000 1 2016 2016
dbSNP: rs1066621
rs1066621
2 1.000 0.080 3 191708066 regulatory region variant C/T snv 0.39 0.700 1.000 1 2018 2018
dbSNP: rs10774021
rs10774021
4 1.000 0.080 12 240132 intron variant C/T snv 0.57 0.700 1.000 1 2010 2010
dbSNP: rs1077989
rs1077989
3 1.000 0.080 14 67509105 intron variant A/C snv 0.39 0.700 1.000 1 2018 2018
dbSNP: rs10783124
rs10783124
1 1.000 0.080 1 99937719 intergenic variant A/G snv 2.9E-02 0.700 1.000 1 2019 2019
dbSNP: rs10794720
rs10794720
4 1.000 0.080 10 1110225 intron variant T/C snv 0.89 0.700 1.000 1 2010 2010
dbSNP: rs10808565
rs10808565
2 0.925 0.080 8 127995166 non coding transcript exon variant C/T snv 0.31 0.010 1.000 1 2007 2007
dbSNP: rs10906850
rs10906850
2 1.000 0.080 10 15183055 regulatory region variant T/C snv 0.29 0.700 1.000 1 2019 2019
dbSNP: rs11011653
rs11011653
2 1.000 0.080 10 19875064 intron variant A/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs11089781
rs11089781
2 0.925 0.080 22 36160720 stop gained G/A snv 1.6E-02 6.5E-02 0.010 1.000 1 2018 2018
dbSNP: rs11123169
rs11123169
3 1.000 0.080 2 113209498 upstream gene variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs11128347
rs11128347
1 1.000 0.080 3 73570410 intron variant G/C;T snv 0.13 0.700 1.000 1 2011 2011
dbSNP: rs112201728
rs112201728
2 1.000 0.080 6 160130454 intron variant C/A;T snv 0.700 1.000 1 2018 2018