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: rs3733590
rs3733590
3 0.925 0.120 4 9985602 intron variant T/C snv 9.5E-02 0.700 1.000 1 2018 2018
dbSNP: rs9992406
rs9992406
3 0.925 0.120 4 9984664 intron variant C/A;T snv 0.23 0.700 1.000 1 2009 2009
dbSNP: rs17246501
rs17246501
3 0.925 0.120 4 9984086 intron variant A/C snv 0.42 0.700 1.000 1 2009 2009
dbSNP: rs7680126
rs7680126
3 0.925 0.120 4 9983972 intron variant G/A snv 0.80 0.800 1.000 2 2009 2015
dbSNP: rs7660895
rs7660895
5 0.882 0.200 4 9983821 intron variant A/G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs11723591
rs11723591
3 0.925 0.120 4 9983774 intron variant T/A snv 0.42 0.700 1.000 1 2009 2009
dbSNP: rs7679724
rs7679724
1 4 9983752 intron variant G/T snv 0.65 0.700 1.000 3 2018 2019
dbSNP: rs10033612
rs10033612
3 0.925 0.120 4 9983382 intron variant C/T snv 0.20 0.700 1.000 1 2009 2009
dbSNP: rs9994216
rs9994216
1 4 9982917 intron variant G/T snv 0.65 0.700 1.000 1 2019 2019
dbSNP: rs10003001
rs10003001
3 0.925 0.120 4 9982851 intron variant C/T snv 0.21 0.700 1.000 1 2009 2009
dbSNP: rs13125646
rs13125646
3 0.925 0.120 4 9980706 synonymous variant A/G;T snv 0.77; 8.0E-06 0.700 1.000 1 2009 2009
dbSNP: rs13115193
rs13115193
3 0.925 0.120 4 9980567 intron variant C/G;T snv 0.47 0.700 1.000 1 2009 2009
dbSNP: rs13125209
rs13125209
3 0.925 0.120 4 9980420 intron variant A/C snv 0.71 0.700 1.000 1 2009 2009
dbSNP: rs13125029
rs13125029
3 0.925 0.120 4 9980405 intron variant A/G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs13145758
rs13145758
3 0.925 0.120 4 9980373 intron variant G/A;T snv 0.700 1.000 1 2009 2009
dbSNP: rs13131257
rs13131257
3 0.925 0.120 4 9980265 intron variant T/C;G snv 0.700 1.000 1 2009 2009
dbSNP: rs882223
rs882223
3 0.925 0.120 4 9980001 intron variant A/C;T snv 0.700 1.000 1 2009 2009
dbSNP: rs11722229
rs11722229
3 0.925 0.120 4 9979073 intron variant C/A;T snv 0.700 1.000 1 2009 2009
dbSNP: rs11723970
rs11723970
3 0.925 0.120 4 9978838 intron variant T/C snv 0.42 0.700 1.000 1 2009 2009
dbSNP: rs13144899
rs13144899
3 0.925 0.120 4 9977678 intron variant C/T snv 6.2E-02 0.700 1.000 1 2009 2009
dbSNP: rs13103497
rs13103497
3 0.925 0.120 4 9977638 intron variant A/G snv 0.53 0.700 1.000 1 2009 2009
dbSNP: rs16868246
rs16868246
3 0.925 0.120 4 9976681 intron variant C/G snv 0.70 0.700 1.000 1 2009 2009
dbSNP: rs4505821
rs4505821
3 0.925 0.120 4 9976470 intron variant G/A snv 0.20 0.700 1.000 1 2009 2009
dbSNP: rs1071988
rs1071988
3 0.925 0.120 4 9973014 intron variant A/G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs6449202
rs6449202
3 0.925 0.120 4 9972419 intron variant T/A;C snv 0.700 1.000 1 2009 2009