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: rs11230201
rs11230201
2 1.000 0.080 11 60229521 intron variant C/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs11601689
rs11601689
1 1.000 0.080 11 60228793 intron variant G/C snv 0.32 0.700 1.000 1 2011 2011
dbSNP: rs1426250
rs1426250
1 1.000 0.080 11 60233852 intron variant A/G snv 0.32 0.700 1.000 1 2011 2011
dbSNP: rs2015475
rs2015475
1 1.000 0.080 11 60231490 intron variant A/C snv 0.32 0.700 1.000 1 2011 2011
dbSNP: rs2081547
rs2081547
1 1.000 0.080 11 60221957 intron variant C/T snv 0.31 0.700 1.000 1 2011 2011
dbSNP: rs4939320
rs4939320
1 1.000 0.080 11 60214328 intron variant T/C snv 0.33 0.700 1.000 1 2011 2011
dbSNP: rs610352
rs610352
1 1.000 0.080 11 60229495 intron variant G/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs611267
rs611267
1 1.000 0.080 11 60237795 intron variant A/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs611418
rs611418
1 1.000 0.080 11 60243540 intron variant C/T snv 0.67 0.700 1.000 1 2011 2011
dbSNP: rs718376
rs718376
1 1.000 0.080 11 60235462 intron variant G/A snv 0.30 0.700 1.000 1 2011 2011
dbSNP: rs670139
rs670139
3 0.925 0.080 11 60204322 intron variant G/A;T snv 0.030 1.000 3 2016 2019